Medicon Instruments, Inc.
Washington, DC, US
Medicon Instruments, Inc. appears in FDA device records in Washington, DC. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Medicon Instruments, Inc. in 1994.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 6 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K936249 | MEDICON INSTRUMENTS UNIPOLAR COAGULATION ELECTRODES | GEI | Substantially Equivalent | |
| K936246 | MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODES | GEI | Substantially Equivalent | |
| K936262 | DISSECTORS, FORCEPS, SCISSORS, DILATION SETS, AND GALL STONE COLLECTORS | GCJ | Substantially Equivalent | |
| K936247 | MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES | DRC | Substantially Equivalent | |
| K936248 | MEDICON INSTRUMENTS CHOLANGIOGRAPHY NEEDLES, GUIDE TUBES, INJECTION NEEDLES, VERRES INSUFFLATION NEEDLES AND HOLDERS | GCJ | Substantially Equivalent | |
| K936250 | RETRACTORS, SPECULUM, CLIP APPLIER FOR TITANIUM CLIPS, 2-WAY STOP COCK, PALPATION PROBE, KNOT GUIDE, ROEDER LOOP | GCJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
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