Atlas FDA

NEW FUCHSIN SOLUTION

FDA 510(k) clearance K871545 · decided 1987-04-29

Clearance details

K-number
K871545
Device name
NEW FUCHSIN SOLUTION
Applicant
Sigma Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1987-04-14
Decision date
1987-04-29
Days to decision
15 days
Clearance type
Traditional
Product code
IDF
Device class
1
Regulation number
864.1850
Medical specialty
Hematology
Advisory committee
Hematology
Location
St. Louis, MO, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.