Atlas FDA

TEST THROMBIN

FDA 510(k) clearance K930157 · decided 1993-05-14

Clearance details

K-number
K930157
Device name
TEST THROMBIN
Applicant
Behring Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1993-01-13
Decision date
1993-05-14
Days to decision
121 days
Clearance type
Traditional
Product code
GJA
Device class
2
Regulation number
864.7875
Medical specialty
Hematology
Advisory committee
Hematology
Location
Somerville, NJ, 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
T-TEK (K050817)R2 Diagnostics, Inc.2005-12-12
ACCUCLOT THROMBIN TIME REAGENT MODEL A8713/A4589 (K982209)Sigma Diagnostics, Inc.1998-10-15
BC THROMBIN REAGENT (K970645)Behring Diagnostics, Inc.1997-05-19
BIOMERIEUX HEMOLAB THROMBICALCI-TEST (K925493)Biomerieux Vitek, Inc.1994-04-21
THROMBIN CLOT TIME TEST PROCEDURE (K923220)Medical Laboratory Automation Systems, Inc.1992-09-29
THROMBIN CLOTTING TIME REAGENT (K920147)Helena Laboratories1992-05-01
TT AND HNTT BY HEMOCHRON (K900126)International Technidyne Corp.1990-02-05
THROMBIN TIME REAGENT (K894467)Sigma Chemical Co.1989-09-05
FIBRI-PREST/THROMBIN-PREST CONTROLS (K884385)American Bioproducts Co.1988-12-28
THROMBIN-PREST REAGENT KIT (K884384)American Bioproducts Co.1988-12-28
IL SYSTEM 810, ACL AND THE REAGENT SETS (K862301)Instrumentation Laboratory CO1986-09-03
THROMBINEX BOVINE THROMBIN (K845000)Bio/Data Corp.1985-03-26

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
OPUS(R) CEA TEST SYSTEM (P920021/S001)Behring Diagnostics, Inc.1996-02-23