Medicotest, Inc.
Washington, DC, US
Medicotest, Inc. appears in FDA device records in Washington, DC. 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 Medicotest, Inc. between 1982 and 2002. The busiest year on record is 1993, with 3. The most recent is 2002, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 2 |
| 1990 | 2 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 3 |
| 1994 | 1 |
| 1995 | 1 |
| 1996 | 1 |
| 1997 | 3 |
| 1999 | 2 |
| 2000 | 1 |
| 2001 | 1 |
| 2002 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K020382 | BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA | DRX | Substantially Equivalent | |
| K020907 | NEUROLINE, SUBDERMAL NEEDLE ELECTRODES | IKT | Substantially Equivalent | |
| K002079 | MULTI-FUNCTION DEFIBRILLATION ELECTRODE | MKJ | Substantially Equivalent | |
| K001869 | DIAGNOSTIC ELECTROMYOGRAPHY NEEDLE ELECTRODE, DISPOSABLE HYPODERMIC NEEDLE | IKT | Substantially Equivalent | |
| K983689 | BLUE SENSOR SUPATAB,DISPOSABLE ECG ELECTRODES | DRX | Substantially Equivalent | |
| K983597 | NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES | GXZ | Substantially Equivalent | |
| K973529 | NEUROLINE, DISPOSABLE CONCENTRIC NEEDLE ELECTRODES | IKT | Substantially Equivalent | |
| K970639 | NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K | GXY | Substantially Equivalent | |
| K965194 | MEDICOM, TENS ELECTRODES | GXY | Substantially Equivalent | |
| K961643 | MEDICOTEST ECG ELECTRODES | DRX | Substantially Equivalent | |
| K952176 | DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K | GXY | Substantially Equivalent | |
| K941568 | K-10-VS, DA-05-VS, RECORDING ELECTRODES | GXY | Substantially Equivalent | |
| K931430 | CUTANEOUS ELECTRODE | GXY | Substantially Equivalent | |
| K931426 | NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE | GXY | Substantially Equivalent | |
| K926264 | MEDICOTEST SKIN FIX | KGX | Substantially Equivalent | |
| K921579 | BR-50-J DISPOSABLE ECG ELECTRODE | DRX | Substantially Equivalent | |
| K914672 | QR-50-E DISPOSABLE RADIOTRANSLUCENT ECG ELECTRODE | DRX | Substantially Equivalent | |
| K902407 | NF-50-E DISPOSABLE ECG ELECTRODE | DRX | Substantially Equivalent | |
| K901280 | DISPOSIBLE EEG NEEDLE ELECTRODES | GXZ | Substantially Equivalent | |
| K821539 | MEDICOTEST ELECTRODE PASTE | GYB | Substantially Equivalent | |
| K821506 | MEDICOTEST ECG ELECTRODES | DRX | 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
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