SURGICAL DRAPE CLIP #201— 510(k) K790855

Name: FDA 510(k) clearance K790855
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

C. Intl.

FDA 510(k) clearance K790855 for SURGICAL DRAPE CLIP #201, Substantially Equivalent on 1979-08-03. Applicant: C. Intl.. Device class: 1.

Clearance details

Applicant: C. Intl.
Product code: Code GDO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1979-05-04
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GDO

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K926199 — UNICLIP SURGICAL CLIP APPLIER1993-04-20
K890941 — MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APP1989-04-07
K890159 — TOWEL CLIPS1989-02-03
K890233 — SUTURE CLIP APPLIER/REMOVER1989-01-27
K820837 — DISPOSABLE MULTIPLE LIGATING CLIP1982-05-28

More clearances from C. Intl.

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K792494 — CATHETERIZATION FORCEP1979-12-20
K790851 — VAGI-PRESS #4011979-07-30
K790852 — VAGI-SPEC1979-07-30
K790853 — EASY-SPEC1979-07-30
K790854 — FORCEPS #101 AND #1021979-06-05

Adverse events under product code GDO

product code GDO

Death: 5
Malfunction: 2,124
Total: 2,129

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.