Atlas FDA

PHARMACIA MUMPS IGG ELISA

FDA 510(k) clearance K897006 · decided 1990-07-26

Clearance details

K-number
K897006
Device name
PHARMACIA MUMPS IGG ELISA
Applicant
Pharmacia Eni Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1989-12-18
Decision date
1990-07-26
Days to decision
220 days
Clearance type
Traditional
Product code
LJY
Device class
1
Regulation number
866.3380
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Columbia, MD, 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
MUMPS IGG ELISA TEST SYSTEM (K991274)Columbia Bioscience, Inc.1999-09-03
SERAQUEST MUMPS IGG (K980059)Quest Intl., Inc.1998-04-23
MUMPS IGG ELISA TESTY (K971857)Gull Laboratories, Inc.1997-11-04
MUMPS IGG TEST (K961204)Zeus Scientific, Inc.1996-07-18
MUMPS STAT (K925209)Biowhittaker Molecular Applications, Inc.1994-10-14
VITEK IMMUNODIAGNOSTIC ASSAY SYSTEM MUMPS IGG ASSA (K923903)Biomerieux Vitek, Inc.1993-08-09
MUMPSELISA TEST KIT (K830045)M.A. Bioproducts1983-05-13

Recalls involving this device

No recalls on record reference this clearance.