MEDICINE CUP— 510(k) K791345

Name: FDA 510(k) clearance K791345
Creator: U.S. Food and Drug Administration
Published: 1979-08-03

Substantially Equivalent

General Clinical Plastics Corp.

FDA 510(k) clearance K791345 for MEDICINE CUP, Substantially Equivalent on 1979-08-03. Applicant: General Clinical Plastics Corp.. Device class: 1.

Clearance details

Applicant: General Clinical Plastics Corp.
Product code: Code KYW
Device class: Class 1
Regulation: 21 CFR 880.6430
Advisory panel: General Hospital
Date received: 1979-07-12
Decision date: 1979-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K800213 — PHARMACY ADDITIVE SYRINGE SET1980-02-26

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K792211 — SPECIMAN CUP & EMESIS BASIN1979-11-16
K791348 — ROUND WASHBASIN & RECTANGLE WASHBASIN1979-09-17
K791346 — DISPOSABLE BEDPAN1979-08-03

Adverse events under product code KYW

product code KYW

Other: 1
Total: 1

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.