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510(k) K894780

IMMUNO/ASO by Immunostics Co., Inc. — Product Code GTQ

K894780 is an FDA 510(k) premarket notification submitted by Immunostics Co., Inc. for the device "IMMUNO/ASO". The FDA issued a decision of Substantially Equivalent on October 16, 1989. The device falls under product code GTQ (Antistreptolysin - Titer/Streptolysin O Reagent), a Class I device regulated under 21 CFR 866.3720. Immunostics Co., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 16, 1989
Date Received
July 27, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antistreptolysin - Titer/Streptolysin O Reagent
Device Class
Class I
Regulation Number
866.3720
Review Panel
MI
Submission Type

Other clearances by Immunostics Co., Inc.

  • K926569 — IMMUNO RA UNDILUTED (April 6, 1993)
  • K902360 — HEMA-SCREEN (July 27, 1990)
  • K883685 — IMMUNO/FEBRILE ANTIGENS (September 28, 1988)
  • K872910 — IMMUNO/SLE (August 12, 1987)
  • K863741 — IMMUNO-CEPT D (BETA-MONOCLONAL) (November 13, 1986)
  • K854619 — DETECTACULT (March 3, 1986)
  • K853105 — IMMUNO-IM (September 3, 1985)
  • K842110 — SLIDE PREGNANCY TEST (July 12, 1984)
  • K834390 — IMMUNO-CRP (February 3, 1984)
  • K834391 — IMMUNO-RA (February 3, 1984)

Other clearances for product code GTQ

  • K052645 — VITROS CHEMISTRY PRODUCTS CALIBRATOR KIT 28, REF 680 2323; VITROS CHEMISTRY PROD (December 14, 2005)
  • K953437 — OLYMPUS ANTI-STERPTOLYSIN O IMMUNOTURBIDIMETRIC REAGENT (October 20, 1995)
  • K915742 — TURBIQUANT ASL (June 28, 1993)
  • K926236 — BECKMAN ANTI-STREPTOLYSIN O KIT (June 15, 1993)
  • K924247 — ACCUTEX ASO LATEX TEST (December 7, 1992)
  • K922723 — TECH SIMPLE ANTISTREPTOLYSIN O ASO SERUM CONTROL (September 18, 1992)
  • K915053 — BECKMAN ANTISTREPTOLYSIN O, MODIFICATION (March 19, 1992)
  • K912150 — BECKMAN ANTI-STREPTOLYSIN O (ASO) KIT (July 17, 1991)
  • K904416 — CROATEST (R) RHEUMATOID DIAGNOSTIC (June 24, 1991)
  • K910885 — QM300 CALIBRATOR G PACK (June 17, 1991)

FDA data resources