Atlas FDA

BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.

FDA 510(k) clearance K802451 · decided 1981-01-09

Clearance details

K-number
K802451
Device name
BLF EIKEN KIT DETER. OF B-LIPOPR. FRAC.
Applicant
Syn-Kit, Inc.
Decision
Substantially Equivalent
Date received
1980-10-08
Decision date
1981-01-09
Days to decision
93 days
Clearance type
Traditional
Product code
JHQ
Device class
1
Regulation number
862.1475
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.