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510(k) K945839

SAS(TM) QC ANTIGENS FOR SALMONELLA ANTISERA by Sa Scientific, Inc. — Product Code GRL

K945839 is an FDA 510(k) premarket notification submitted by Sa Scientific, Inc. for the device "SAS(TM) QC ANTIGENS FOR SALMONELLA ANTISERA". The FDA issued a decision of Substantially Equivalent on March 7, 1995. The device falls under product code GRL (Antigens, All Groups, Salmonella Spp.), a Class II device regulated under 21 CFR 866.3550. Sa Scientific, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 1995
Date Received
November 30, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigens, All Groups, Salmonella Spp.
Device Class
Class II
Regulation Number
866.3550
Review Panel
MI
Submission Type

Other clearances by Sa Scientific, Inc.

  • K132352 — SAS FLUALERT A & B, SAS INFLUENZA A TEST (August 22, 2013)
  • K100227 — SAS FLUALERT A&B, SAS INFLUENZA A TEST (February 23, 2010)
  • K080380 — SAS INFLUENZA A & B TEST (July 23, 2009)
  • K061496 — SAS LEGIONELLA TEST, SAS LEGIONELLA DIPSTICK TEST (June 28, 2007)
  • K041441 — SAS INFLUENZA A TEST (July 22, 2004)
  • K041439 — SAS INFLUENZA B TEST (July 22, 2004)
  • K030628 — SAS RSV CONTROL KIT (March 17, 2003)
  • K022845 — SAS RSV TEST (January 29, 2003)
  • K022683 — SAS BLOOD/SERUM/URINE/URINE HCG (December 16, 2002)
  • K023270 — SAS STREPALERT (October 17, 2002)

Other clearances for product code GRL

  • K820996 — SALMONELLA & SHIGELLA GROUPING SERA (May 3, 1982)

FDA data resources