Everest Medical Corp.
Minneapolis, MN, US
Everest Medical Corp. appears in FDA device records in Minneapolis, MN. FDA records list 21 510(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
- 21
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 21 510(k) clearances for Everest Medical Corp. between 1987 and 2000. The busiest year on record is 1991, with 6. The most recent is 2000, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1987 | 1 |
| 1989 | 3 |
| 1990 | 1 |
| 1991 | 6 |
| 1992 | 3 |
| 1994 | 1 |
| 1995 | 1 |
| 1998 | 1 |
| 2000 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K003060 | PLASMAKINETIC GENERATOR | GEI | Substantially Equivalent | |
| K000496 | EVERSHEARS BIPOLAR SCISSORS | GEI | Substantially Equivalent | |
| K993412 | BITX PROBES | GEI | Substantially Equivalent | |
| K994336 | BITX PROBES | GEI | Substantially Equivalent | |
| K971565 | BICOAG COAGULATING FORCEPS | HIN | Substantially Equivalent | |
| K955001 | EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS | GEI | Substantially Equivalent | |
| K945975 | EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS | GEI | Substantially Equivalent | |
| K922509 | LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA | GEI | Substantially Equivalent | |
| K922246 | TUBING SET W/ IRRIGATION & ASPIRATION VALVING | GCJ | Substantially Equivalent | |
| K920089 | MONOPOLAR COAGULATING POLYPECTOMY SNARE | KNS | Substantially Equivalent | |
| K911787 | MONOPOLAR SPHINCTERTOME | GEI | Substantially Equivalent | |
| K911700 | MONOPOLAR POLLYPECTOMY SNARE | KNS | Substantially Equivalent | |
| K912544 | BIPOLAR FORCEPS | MAV | Substantially Equivalent | |
| K905714 | ERCP CANNULA | FGE | Substantially Equivalent | |
| K904993 | LAPAROSCOPIC ELECTROSURGICAL DEVICE | GEI | Substantially Equivalent | |
| K904985 | BIPOLAR BIOPSY FORCEPS | KGE | Substantially Equivalent | |
| K895842 | BITOME(TM) BIPOLAR SPHINCTEROTOME | KNS | Substantially Equivalent | |
| K895841 | MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. | GEI | Substantially Equivalent | |
| K892895 | MODEL 8800 BIPOLAR COAGULATION THERAPEUTIC SYSTEM | KNS | Substantially Equivalent | |
| K893553 | BIPOLAR ELECTROSURGICAL SNARE | FDI | Substantially Equivalent | |
| K870981 | MODEL 8700 BIPOLAR ELECTROSURGICAL GENERATOR | GEI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HINCoagulator-Cutter, Endoscopic, Bipolar (And Accessories)
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- KGEForceps, Biopsy, Electric
- GCJLaparoscope, General & Plastic Surgery
- FDISnare, Flexible
- FGEStents, Drains And Dilators For The Biliary Ducts
- MAVSyringe, Balloon Inflation
- KNSUnit, Electrosurgical, Endoscopic (With Or Without 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.
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Data as of , FDA export datePage updated Source: openFDA, public domain
