Atlas FDA

RUBA-NOST TEST KITS

FDA 510(k) clearance K771796 · decided 1977-10-18

Clearance details

K-number
K771796
Device name
RUBA-NOST TEST KITS
Applicant
Behring Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1977-09-23
Decision date
1977-10-18
Days to decision
25 days
Clearance type
Traditional
Product code
GOL
Device class
2
Regulation number
866.3510
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, 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
RUBELLA ANTIBODY FLUOROIMMUNOASSAY (K841174)Intl. Diagnostic Technology1984-06-07
RUBAQUICK DIAGNOSTIC KIT (K834032)Abbott Laboratories1984-04-17
RUBELLA ANTIBODIES TEST REAGENTS (K810309)Calbiochem-Behring Corp.1981-03-11
RUBELISA IGM TEST KIT (K802508)M.A. Bioproducts1980-12-18
RUBELLA ELISA REAGENTS RUBELLA IGG ANTI (K802102)Calbiochem-Behring Corp.1980-12-18
EIA RUBELLA-G (K802339)Beckman Instruments, Inc.1980-12-18
GAMMA COAT(125 I) RUBELLA ANTIBODY (K801667)Clinical Assays, Inc.1980-10-23
ENZYME-IMMUNOASSAY (RUBELLA ANTIBODIES) (K801098)Flow Laboratories, Inc.1980-09-16
ANTIGEN CONTROL CELLS (K801507)Ortho Diagnostics, Inc.1980-08-20
RUBELLA BIO-BEAD TITRATION KIT (K800789)Litton Bionetics1980-06-30
MACRO-VUE RUBELLA CARD TEST (K800797)Bd Becton Dickinson Vacutainer Systems Preanalytic1980-06-20
FIAX TEST KIT FOR ANTI-RUBELLA ANTIBOD (K792249)Intl. Diagnostic Technology1980-01-23

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