Atlas FDA

MICROTRAK NEISERRIA GONORRHOEAE CULTURE TEST

FDA 510(k) clearance K861835 · decided 1986-05-29

Clearance details

K-number
K861835
Device name
MICROTRAK NEISERRIA GONORRHOEAE CULTURE TEST
Applicant
Syva Co.
Decision
Substantially Equivalent
Date received
1986-05-13
Decision date
1986-05-29
Days to decision
16 days
Clearance type
Traditional
Product code
GTH
Device class
2
Regulation number
866.3390
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Palo Alto, 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
BARTELS NEISSERIA GONORRHOEAE DIRECT FLUORESCENT (K900546)Baxter Healthcare Corp1990-06-15
NEISSERIA GONORRHOEAE FLUORO-KIT (K800328)Clinical Sciences, Inc.1980-03-03

Recalls involving this device

No recalls on record reference this clearance.