Atlas FDA

QUANTA LITE GPA (GASTRIC PARIETAL CELL ANTIBODY) ELISA

FDA 510(k) clearance K010558 · decided 2001-04-03

Clearance details

K-number
K010558
Device name
QUANTA LITE GPA (GASTRIC PARIETAL CELL ANTIBODY) ELISA
Applicant
Inova Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
2001-02-26
Decision date
2001-04-03
Days to decision
36 days
Clearance type
Traditional
Product code
MLE
Device class
2
Regulation number
866.5110
Medical specialty
Immunology
Advisory committee
Immunology
Location
San Diego, CA, 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
AUTOSTAT II ANTI-GPC ELISA, HY.TEC ANTI-GPC ELISA (K991942)Cogent Diagnotics , Ltd.1999-08-24
VARELISA PARIETAL CELL ANTIBODIES (K951206)Elias U.S.A., Inc.1995-04-17

Recalls involving this device

No recalls on record reference this clearance.