Atlas FDA

SUCTION RETRACTOR

FDA 510(k) clearance K875289 · decided 1988-01-22

Clearance details

K-number
K875289
Device name
SUCTION RETRACTOR
Applicant
T. Korossurgical Instruments Corp.
Decision
Substantially Equivalent
Date received
1987-12-30
Decision date
1988-01-22
Days to decision
23 days
Clearance type
Traditional
Product code
GAD
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Moorepark, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.