Atlas FDA

COUNT-10 STAIN

FDA 510(k) clearance K823363 · decided 1982-12-15

Clearance details

K-number
K823363
Device name
COUNT-10 STAIN
Applicant
V-Tech, Inc.
Decision
Substantially Equivalent
Date received
1982-11-09
Decision date
1982-12-15
Days to decision
36 days
Clearance type
Traditional
Product code
LEE
Device class
1
Regulation number
864.1850
Medical specialty
Hematology
Advisory committee
Hematology
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.