Amsco Co.
Mchenry, IL, US
Amsco Co. appears in FDA device records in Mchenry, IL. FDA records list 13 510(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
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Amsco Co. between 1977 and 1983. The busiest year on record is 1983, with 5. The most recent is 1983, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 3 |
| 1978 | 2 |
| 1980 | 2 |
| 1981 | 1 |
| 1983 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K833187 | HALL OSTEON | GET | Substantially Equivalent | |
| K832188 | HALL RECIPROCATOR | GET | Substantially Equivalent | |
| K832187 | HALL OSCILLATOR | GET | Substantially Equivalent | |
| K832186 | HALL DRILL/REAMER | GET | Substantially Equivalent | |
| K831309 | DELIVERY 4 TABLE | KNC | Substantially Equivalent | |
| K811242 | DISPOSABLE STERILIZATION WRAP | FRG | Substantially Equivalent | |
| K802838 | STERNUM SAW BLADE | GFA | Substantially Equivalent | |
| K801109 | PROOF (BIOLOGICAL/CHEMICAL INDICATOR) | JOJ | Substantially Equivalent | |
| K782064 | TABLE, EXAMINING-TWO EIGHTY | ETF | Substantially Equivalent | |
| K780771 | MICRO RASPS | HTR | Substantially Equivalent | |
| K772135 | BIOLOGICAL/CHEMICAL INDICATOR | JOJ | Substantially Equivalent | |
| K761341 | PORTAGAS AERATOR | FLI | Substantially Equivalent | |
| K761018 | SURGICAL LIGHT - CHALLENGE 22 SERIES | FQP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- GFABlade, Saw, General & Plastic Surgery, Surgical
- FLICabinet, Ethylene-Oxide Gas Aerator
- JOJIndicator, Physical/Chemical Sterilization Process
- FQPLamp, Operating-Room
- GETMotor, Surgical Instrument, Pneumatic Powered
- HTRRasp
- KNCTable, Obstetric (And Accessories)
- ETFUnit, Examining/Treatment, Ent
- FRGWrap, Sterilization
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain
