SAS SALMONELLA H Z42 ANTISERUM— 510(k) K961955

Name: FDA 510(k) clearance K961955
Creator: U.S. Food and Drug Administration
Published: 1996-06-18

Substantially Equivalent

Sa Scientific, Inc.

FDA 510(k) clearance K961955 for SAS SALMONELLA H Z42 ANTISERUM, Substantially Equivalent on 1996-06-18. Applicant: Sa Scientific, Inc.. Device class: 2.

Clearance details

Applicant: Sa Scientific, Inc.
Product code: Code GRM
Device class: Class 2
Regulation: 21 CFR 866.3550
Advisory panel: Microbiology
Date received: 1996-05-20
Decision date: 1996-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GRM

view all

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 Sa Scientific, Inc.

view all

K100227 — SAS FLUALERT A&B, SAS INFLUENZA A TEST2010-02-23
K080380 — SAS INFLUENZA A & B TEST2009-07-23
K041439 — SAS INFLUENZA B TEST2004-07-22
K041441 — SAS INFLUENZA A TEST2004-07-22
K030628 — SAS RSV CONTROL KIT2003-03-17

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