Applied Medical Technologies
Mchenry, IL, US
Applied Medical Technologies appears in FDA device records in Mchenry, IL. FDA records list 24 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for Applied Medical Technologies between 1981 and 1998. The busiest year on record is 1989, with 7. The most recent is 1998, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1981 | 1 |
| 1989 | 7 |
| 1990 | 3 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 1 |
| 1995 | 3 |
| 1996 | 2 |
| 1997 | 3 |
| 1998 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K971434 | A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICE | KNT | Substantially Equivalent | |
| K972478 | PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES | KNT | Substantially Equivalent | |
| K973893 | AMT BALLOON STOMA MEASURING DEVICES, AMT BALLOON MEASURING DEVICE, AMT BALLOON MEASURING DEVICE WITH STOP VALVE, AMY BAE | KNT | Substantially Equivalent | |
| K971757 | LOW PROFILE FEEDING SET ACCESSORY | KNT | Substantially Equivalent | |
| K971758 | CAUTERIZATION SMOKE EVACUATOR | GEI | Substantially Equivalent | |
| K961345 | DOMED PERCUTANEOUS ENDOSCOPIC GASTROSTOMY(P.E.G.) FEEDING TUBE | KNT | Substantially Equivalent | |
| K960232 | ENDOSCOPIC ACCESS DEVICE | GCJ | Substantially Equivalent | |
| K945618 | GASTROINTESTINAL TUBES & ACCESSORIES | KNT | Substantially Equivalent | |
| K946140 | PRG BUTTON | KNT | Substantially Equivalent | |
| K923488 | GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY | KNT | Substantially Equivalent | |
| K923692 | STOMA MEASURING DEVICE | KNT | Unknown | |
| K920894 | DECOMPRESSION TUBES | KNT | Substantially Equivalent | |
| K910584 | ONE STEP BUTTON(TM) | KGC | Substantially Equivalent | |
| K903036 | P.R.G. GUIDEWIRE PLACEMENT SYSTEM | KGC | Unknown | |
| K900884 | P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY | KGC | Unknown | |
| K901339 | BIOPSY FORCEPS (NON-RIGID) | KNW | Substantially Equivalent | |
| K895480 | BLUNT NEEDLE PORT/I.V. PORT | FPA | Substantially Equivalent | |
| K895684 | SOFT SUCTION ADAPTER | GEA | Substantially Equivalent | |
| K895727 | BACKGROUND SUCTION MATT | NAB | Substantially Equivalent | |
| K895726 | VESSEL OCCLUDER | GDJ | Substantially Equivalent | |
| K895683 | BERNARD VESSEL APPROXIMATOR | HRQ | Substantially Equivalent | |
| K895682 | VESSEL LOOPS | GDX | Substantially Equivalent | |
| K895681 | CONTRAST BACKGROUND MATERIAL | GAB | Substantially Equivalent | |
| K810203 | MODEL AM 722 | JFP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GEACannula, Surgical, General & Plastic Surgery
- GDJClamp, Surgical, General & Plastic Surgery
- JFPElectrode, Ion Specific, Calcium
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- NABGauze / Sponge,Nonresorbable For External Use
- HRQHemostat
- KNWInstrument, Biopsy
- GCJLaparoscope, General & Plastic Surgery
- GABNeedle, Suturing, Disposable
- GDXScalpel, One-Piece
- FPASet, Administration, Intravascular
- KGCTube, Gastro-Enterostomy
- KNTTubes, Gastrointestinal (And Accessories)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Applied Medical Technologies edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Applied Medical Technologies. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain