Atlas FDA

WAKO NEFA LINEARITY SET

FDA 510(k) clearance K973072 · decided 1997-09-12

Clearance details

K-number
K973072
Device name
WAKO NEFA LINEARITY SET
Applicant
Wako Chemicals USA, Inc.
Decision
Substantially Equivalent
Date received
1997-08-18
Decision date
1997-09-12
Days to decision
25 days
Clearance type
Traditional
Product code
JJX
Device class
1
Regulation number
862.1660
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Richmond, VA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.