Atlas FDA

IFA FOR CHLAMYDIA TRACHOMATIS IGG ANTIBODY

FDA 510(k) clearance K914953 · decided 1992-02-19

Clearance details

K-number
K914953
Device name
IFA FOR CHLAMYDIA TRACHOMATIS IGG ANTIBODY
Applicant
Stellar Bio Systems, Inc.
Decision
Substantially Equivalent
Date received
1991-11-05
Decision date
1992-02-19
Days to decision
106 days
Clearance type
Traditional
Product code
LKI
Device class
1
Regulation number
866.3120
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
LUPUS(LE)-LATEX TEST (K905531)Immco Diagnostics, Inc.1991-01-25
CHLAMYDIA (LGV-1) (K894625)Bion Ent., Ltd.1989-08-15
BTC CHLAMYDIA DIRECT SPECIMEN TEST & CONTROL SLIDE (K883776)Btc Corp.1989-02-03
MONABRITE CHLAMYDIA TRACH CULTURE CONFIRMATION TES (K854615)Serono Diagnostics, Inc.1986-01-28
CULUTURE SET CHLAMYDIA ISOLATION AND (K830342)Immulok, Inc.1983-05-04

Recalls involving this device

No recalls on record reference this clearance.