510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952141Substantially Equivalent

Sas Francisella Tularensis Antiserum

SA Scientific, Ltd, San Antonio TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952141 is the FDA 510(k) clearance record for SAS FRANCISELLA TULARENSIS ANTISERUM, a class II device, cleared for Sa Scientific, Inc. on under FDA product code GSK (Antiserum, Francisella Tularensis). FDA records list 201 510(k) clearances for Sa Scientific, Inc., from to . As of , FDA records show no recalls naming K952141.

Clearance record

Decision date
Received
(74 days to decision)
Product code
GSK Antiserum, Francisella Tularensis
Regulation
21 CFR 866.3280
Device class
Class II
Review panel
Microbiology
Applicant
Sa Scientific, Inc. 4919 Golden Quail, San Antonio TX
510(k) summary
Statement
Third party review
No

Clearances, product code GSK

Trailing 12 months

FDA records hold no clearances under product code GSK in the trailing twelve months.

FDA records show no clearances under product code GSK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GSK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260