Atlas FDA

BLASTOMYCES DERMATITIDIS, ANTIGEN

FDA 510(k) clearance K792680 · decided 1980-01-17

Clearance details

K-number
K792680
Device name
BLASTOMYCES DERMATITIDIS, ANTIGEN
Applicant
Meridian Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1979-12-27
Decision date
1980-01-17
Days to decision
21 days
Clearance type
Traditional
Product code
JWW
Device class
2
Regulation number
866.3060
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Meridian Diagnostics

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
IMMUNODIFFUSSION REAGENTS/SEROLOGICAL (K802128)Nolan Biological Laboratories, Inc.1980-09-26
BLASTOMYCES/ANTIGEN FOR IMMUNODIFUSION (K792683)Meridian Diagnostics, Inc.1980-01-23

Recalls involving this device

No recalls on record reference this clearance.