Atlas FDA

WAKO TOTAL BILIRUBIN V

FDA 510(k) clearance K970985 · decided 1997-04-21

Clearance details

K-number
K970985
Device name
WAKO TOTAL BILIRUBIN V
Applicant
Wako Chemicals USA, Inc.
Decision
Substantially Equivalent
Date received
1997-03-18
Decision date
1997-04-21
Days to decision
34 days
Clearance type
Traditional
Product code
JFM
Device class
2
Regulation number
862.1110
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Richmond, VA, US
Third-party review
No
Expedited review
No

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ENZYMATIC BILIRUBIN (TOTAL), CATALOGUE NO. 202-14 (K904660)Diagnostic Chemicals, Ltd. (Usa)1990-11-20
DRI-STAT ENZYMATIC BILIRUBIN TEST KIT (K843174)Beckman Instruments, Inc.1984-09-14

Recalls involving this device

No recalls on record reference this clearance.