Atlas FDA

AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*

FDA 510(k) clearance K904931 · decided 1991-01-29

Clearance details

K-number
K904931
Device name
AUTO SUTURE(R) PERMANENT PURSTRING(TM) APPLIER*
Applicant
United States Surgical, A Division of Tyco Healthc
Decision
Substantially Equivalent
Date received
1990-10-31
Decision date
1991-01-29
Days to decision
90 days
Clearance type
Traditional
Product code
GAR
Device class
2
Regulation number
878.5020
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Norwalk, CT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.