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510(k) K790854

FORCEPS #101 AND #102 by C. Intl. — Product Code GEN

K790854 is an FDA 510(k) premarket notification submitted by C. Intl. for the device "FORCEPS #101 AND #102". The FDA issued a decision of Substantially Equivalent on June 5, 1979. The device falls under product code GEN (Forceps, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. C. Intl. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 5, 1979
Date Received
May 4, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by C. Intl.

  • K792494 — CATHETERIZATION FORCEP (December 20, 1979)
  • K790855 — SURGICAL DRAPE CLIP #201 (August 3, 1979)
  • K790853 — EASY-SPEC (July 30, 1979)
  • K790852 — VAGI-SPEC (July 30, 1979)
  • K790851 — VAGI-PRESS #401 (July 30, 1979)
  • K790856 — PROCTOSCOPE #501 (May 29, 1979)

Other clearances for product code GEN

  • K031828 — NATURALASE LP ND:YAG LASER (July 17, 2003)
  • K953962 — FORCEPS (September 8, 1995)
  • K932385 — SUTURE REMOVING FORCEPS (August 6, 1993)
  • K904723 — FORCEPS (July 26, 1991)
  • K911159 — PALPATION PROBE (March 29, 1991)
  • K900951 — GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIP (April 18, 1990)
  • K900948 — GS-1002 GRASPING FORCEP, 5MM WITH RATCHET (April 18, 1990)
  • K900960 — GS-1500 CLAW FORCEP, 10MM (April 18, 1990)
  • K900952 — GS-1200 GRASPING/EXTRACTING FORCEP, 10MM (April 18, 1990)
  • K891896 — TISSUE FORCEPS, VARIOUS TYPES (April 12, 1989)

FDA data resources