Atlas FDA

INFLUENZA HA ANTIGEN A/USSR

FDA 510(k) clearance K780275 · decided 1978-02-28

Clearance details

K-number
K780275
Device name
INFLUENZA HA ANTIGEN A/USSR
Applicant
Flow Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1978-02-17
Decision date
1978-02-28
Days to decision
11 days
Clearance type
Traditional
Product code
GNT
Device class
1
Regulation number
866.3330
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
VIRAZYME CULTURE CONFIRMATION SCREEN FOR INFLUENZA AND PARAINFLUENZA VIRUSES (K950838)Zymetx, Inc.1996-06-17
QTEST INFLUENZA A (K913828)Bd Becton Dickinson Vacutainer Systems Preanalytic1991-09-23
DIRECTIGEN FLU A (K902609)Bd Becton Dickinson Vacutainer Systems Preanalytic1990-09-10
INFLUENZA HA ANTIGEN (K780272)Flow Laboratories, Inc.1978-02-28

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
3M BRAND MICROBIAL PROFILE SYSTEM (N50538/S001)Flow Laboratories, Inc.1981-04-17
FLOW MIC SYSTEM (N50538)Flow Laboratories, Inc.1980-07-15