Home / 510(k) Clearances / K790855

510(k) K790855

SURGICAL DRAPE CLIP #201 by C. Intl. — Product Code GDO

K790855 is an FDA 510(k) premarket notification submitted by C. Intl. for the device "SURGICAL DRAPE CLIP #201". The FDA issued a decision of Substantially Equivalent on August 3, 1979. The device falls under product code GDO (Applier, Surgical, Clip), 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
August 3, 1979
Date Received
May 4, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Applier, Surgical, Clip
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by C. Intl.

  • K792494 — CATHETERIZATION FORCEP (December 20, 1979)
  • K790853 — EASY-SPEC (July 30, 1979)
  • K790852 — VAGI-SPEC (July 30, 1979)
  • K790851 — VAGI-PRESS #401 (July 30, 1979)
  • K790854 — FORCEPS #101 AND #102 (June 5, 1979)
  • K790856 — PROCTOSCOPE #501 (May 29, 1979)

Other clearances for product code GDO

  • K926199 — UNICLIP SURGICAL CLIP APPLIER (April 20, 1993)
  • K890941 — MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APP (April 7, 1989)
  • K890159 — TOWEL CLIPS (February 3, 1989)
  • K890233 — SUTURE CLIP APPLIER/REMOVER (January 27, 1989)
  • K820837 — DISPOSABLE MULTIPLE LIGATING CLIP (May 28, 1982)
  • K812291 — ETHICON MULTIPLE LIGATING CLIP APPLIER (September 11, 1981)
  • K792378 — HEMOSPENSER CARTRIDGE CAT. NO. 523500- (December 6, 1979)
  • K791845 — BAYONET HEIFETZ CLIP APPLIERS (October 17, 1979)
  • K791157 — 360 HEMOCLIP APPLIERS (June 27, 1979)
  • K790990 — REYNOLDS DOUBLE HEMOCLIP APPLIERS (June 5, 1979)

FDA data resources