Atlas FDA

K-ASSAY HAPTOGLOBIN

FDA 510(k) clearance K993480 · decided 1999-11-24

Clearance details

K-number
K993480
Device name
K-ASSAY HAPTOGLOBIN
Applicant
Kamiya Biomedical Co.
Decision
Substantially Equivalent
Date received
1999-10-14
Decision date
1999-11-24
Days to decision
41 days
Clearance type
Traditional
Product code
DAD
Device class
2
Regulation number
866.5460
Medical specialty
Immunology
Advisory committee
Immunology
Location
Seattle, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
TINA-QUANT HAPTOGLOBIN (K972639)Boehringer Mannheim Corp.1998-01-09
N-ASSAY TIA MULTI V-NL (K964301)Crestat Diagnostics, Inc.1997-07-14
IMMAGE IMMUNOCHEMISTRY SYSTEM HAPTOGLOBIN (HPT) REAGENT (K963286)Beckman Instruments, Inc.1996-10-07
N/T PROTEIN CONTROL SY/L, M AND H (K952593)Behring Diagnostics, Inc.1995-07-17
IL TEST(TM) HAPTOGLOBIN (HPT) (K915829)Instrumentation Laboratory CO1992-07-29
RAICHEM(TM) SPIA(TM) HAPTOGLOBIN REAGENT (K911898)Reagents Applications, Inc.1991-05-08
SPQ(TM) ANTIBODY REAGENT SET II FOR HPT (K890562)Atlantic Antibodies1989-02-22
HAPTOGLOBIN (K873866)Unipath , Ltd.1987-10-20
QM300 HAPTOGLOBIN ANTIBODY PACK (K872717)Kallestad Diag, A Div. of Erbamont, Inc.1987-07-21
IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO (K864512)Cooper Biomedical, Inc.1987-02-13
SPQ TEST SYSTEM FOR HAPTOGLOBIN (K850584)Applications Lab1985-03-05
DIFFU-GEN HAPTOGLOBIN RADIAL IMMUNO (K840404)Tago, Inc.1984-03-09

Recalls involving this device

No recalls on record reference this clearance.