Atlas FDA

MUMPS S & V ANTIGENS & CONTROLS

FDA 510(k) clearance K802933 · decided 1980-12-31

Clearance details

K-number
K802933
Device name
MUMPS S & V ANTIGENS & CONTROLS
Applicant
Orion Diagnostica, Inc.
Decision
Substantially Equivalent
Date received
1980-11-19
Decision date
1980-12-31
Days to decision
42 days
Clearance type
Traditional
Product code
GRC
Device class
1
Regulation number
866.3380
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, 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
MUMPS COMPLEMENT-FIXATION (C.F.) ANTIGEN (K905306)Virion (U.S.), Inc.1991-06-17
MUMPS COMPLEMENT FIXATION & HEMAGGLU (K832873)Hazleton Dutchland, Inc.1983-12-27

Recalls involving this device

No recalls on record reference this clearance.