DIPSTICK SALMONELLA— 510(k) K910438

Substantially Equivalent

Ampcor, Inc.

FDA 510(k) clearance K910438 for DIPSTICK SALMONELLA, Substantially Equivalent on 1991-09-13. Applicant: Ampcor, Inc.. Device class: 2.

Clearance details

Applicant: Ampcor, Inc.
Product code: Code GRM
Device class: Class 2
Regulation: 21 CFR 866.3550
Advisory panel: Microbiology
Date received: 1991-01-31
Decision date: 1991-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bridgeport, NJ, US

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Recent devices under product code GRM

K961948 — SAS SALMONELLA O FACTOR 20 ANTISERUM1996-06-18
K961949 — SAS SALMONELLA O FACTOR 14 ANTISERUM1996-06-18
K961950 — SAS SALMONELLA O FACTOR 15 ANTISERUM &/OR O GROUP E2 FACTOR 15 ANTISERUM1996-06-18
K961951 — SAS SALMONELLA O FACTOR 6 ANTISERUM1996-06-18
K961952 — SAS SALMONELLA O FACTOR /O GROUP A FACTOR 2 ANTISERUMS1996-06-18

More clearances from Ampcor, Inc.

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K893873 — SINGLE AND DUAL BAND DIPSTICK HCG TEST1989-08-21
K890048 — QUIK-DOT TOXOPLASMOSIS1989-06-09
K892119 — QUIK-DOT C REACTIVE PROTEIN1989-04-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.