Atlas FDA

CELLMATICS SHLAMYDIA DETECTION SYSTEM

FDA 510(k) clearance K893669 · decided 1989-06-23

Clearance details

K-number
K893669
Device name
CELLMATICS SHLAMYDIA DETECTION SYSTEM
Applicant
Difco Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1989-05-15
Decision date
1989-06-23
Days to decision
39 days
Clearance type
Traditional
Product code
LKH
Device class
1
Regulation number
866.3120
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Detroit, MI, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Difco Laboratories

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
IPAZYME (TM) CHLAMYDIA IGG-IGA (K910644)Savyon Diagnostics , Ltd.1991-03-19
IPAZYME(TM) CHLAMYDIA TRUE IGM(TM) (K901975)Savyon Diagnostics , Ltd.1991-03-08
IMMU-MARK(TM) CHLAMYDIA IGG/IGA KIT (K882674)Icn Immunobiologicals1989-08-15
SELECTICULT-CHLAMYDIA (K852869)Scott Laboratories, Inc.1985-09-19
CHLAMYDIAE IMMUNOPEROXIDASE TEST KIT (K842151)Bartels Immunodiagnostic Supplies, Inc.1984-07-20
COMBION SKIN TEST (K830688)Nicholas H. Maganias1983-03-31
HISTOSET IMMUNOPEROXIDASE TISSURE KIT (K820390)Immulok, Inc.1982-04-14

Recalls involving this device

No recalls on record reference this clearance.