Atlas FDA

SURGICAL INSTRUMENTS

FDA 510(k) clearance K811686 · decided 1981-07-20

Clearance details

K-number
K811686
Device name
SURGICAL INSTRUMENTS
Applicant
C.V.I., Inc.
Decision
Substantially Equivalent
Date received
1981-06-15
Decision date
1981-07-20
Days to decision
35 days
Clearance type
Traditional
Product code
GEN
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
NATURALASE LP ND:YAG LASER (K031828)Focus Medical, LLC2003-07-17
FORCEPS (K953962)Biopsys Medical, Inc.1995-09-08
SUTURE REMOVING FORCEPS (K932385)Rocket of London, Ltd.1993-08-06
FORCEPS (K904723)Minto Research & Development, Inc.1991-07-26
PALPATION PROBE (K911159)Northgate Technologies, Inc.1991-03-29
GS-1002 GRASPING FORCEP, 5MM WITH RATCHET (K900948)Solos Endoscopy, Inc.1990-04-18
GS-1500 CLAW FORCEP, 10MM (K900960)Solos Endoscopy, Inc.1990-04-18
GS-1200 GRASPING/EXTRACTING FORCEP, 10MM (K900952)Solos Endoscopy, Inc.1990-04-18
GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP (K900951)Solos Endoscopy, Inc.1990-04-18
TISSUE FORCEPS, VARIOUS TYPES (K891896)Zinnanti Surgical Instruments, Inc.1989-04-12
HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT (K891401)Zinnanti Surgical Instruments, Inc.1989-04-06
CAMPION LASER FORCEPS (K891348)Simpson/Basye, Inc.1989-03-22

Recalls involving this device

No recalls on record reference this clearance.