Ipco Corp.
Mchenry, IL, US
Ipco Corp. 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 Ipco Corp. between 1976 and 1984. The busiest year on record is 1980, with 4. The most recent is 1984, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 2 |
| 1977 | 1 |
| 1978 | 3 |
| 1979 | 1 |
| 1980 | 4 |
| 1984 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K842838 | SAFE & SOFT PANTY SHIELDS | HHD | Substantially Equivalent | |
| K841953 | ULTRA SHIELD BRIEFS | EYQ | Substantially Equivalent | |
| K800293 | FILE, PULP CANAL | EKS | Substantially Equivalent | |
| K800292 | ENDEX BROACH, ENDODONTIC | EKW | Substantially Equivalent | |
| K800291 | ENDEX REAMERS PULP CANAL, ENDODONTIC | EKP | Substantially Equivalent | |
| K800117 | TRU-PULSE PADS | GXY | Substantially Equivalent | |
| K782164 | STIMULATOR, MODEL 1-600 ELECTRIC NERVR | GZJ | Substantially Equivalent | |
| K781679 | MONITOR/MINI SCOPE | DPS | Substantially Equivalent | |
| K781678 | DEFIBRILLATOR, MARK II | LDD | Substantially Equivalent | |
| K780416 | PANTRIDGE MK III DEFIBRILLATOR/MONITOR | LDD | Substantially Equivalent | |
| K761221 | NON-STERILE PREGELLED GROUNDING PAD | GEI | Substantially Equivalent | |
| K760203 | TUBE, STERILE NON-CONDUCTIVE CONNECTING | GCD | Substantially Equivalent | |
| K760202 | TUBE, STERILE CONDUCTIVE CONNECTING | GAZ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EKWBroach, Endodontic
- GCDConnector, Catheter
- LDDDc-Defibrillator, Low-Energy, (Including Paddles)
- DPSElectrocardiograph
- GXYElectrode, Cutaneous
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- EKSFile, Pulp Canal, Endodontic
- EYQGarment, Protective, For Incontinence
- HHDPad, Menstrual, Unscented
- EKPReamer, Pulp Canal, Endodontic
- GZJStimulator, Nerve, Transcutaneous, For Pain Relief
- GAZTubing, Noninvasive
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain