Atlas FDA

QUANTA LITE SLA (SOLUBLE LIVER ANTIGEN) ELISA

FDA 510(k) clearance K021482 · decided 2002-07-30

Clearance details

K-number
K021482
Device name
QUANTA LITE SLA (SOLUBLE LIVER ANTIGEN) ELISA
Applicant
Inova Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
2002-05-08
Decision date
2002-07-30
Days to decision
83 days
Clearance type
Traditional
Product code
NIY
Device class
2
Regulation number
866.5660
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
EUROIMMUN EUROLINE PROFILE AUTOIMMUNE LIVER DISEASE 8AG (IGG) (K113439)Euroimmun US2013-04-12
EUROIMMUN ANTI-SLA/LP ELISA(LGG) (K112221)Euroimmun US2012-09-11

Recalls involving this device

No recalls on record reference this clearance.