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FDA 510(k)

MEDICINE CUP

K-Number: K791345 · 1979-08-03

ApplicantGeneral Clinical Plastics Corp.
Decision Date1979-08-03
Product CodeKYW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDICINE CUP is the device name listed in this FDA 510(k) record. The listed applicant is General Clinical Plastics Corp.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791345. The device is classified under product code KYW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICINE CUP?

MEDICINE CUP is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is General Clinical Plastics Corp.. The 510(k) number is K791345.

When did MEDICINE CUP receive FDA 510(k) clearance?

MEDICINE CUP received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791345.

Who is the listed applicant for MEDICINE CUP?

The FDA 510(k) record lists General Clinical Plastics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDICINE CUP?

The FDA product code for MEDICINE CUP is KYW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing General Clinical Plastics Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K792211SPECIMAN CUP & EMESIS BASINK791348ROUND WASHBASIN & RECTANGLE WASHBASINK791346DISPOSABLE BEDPAN

Related Devices (Code: KYW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K800213PHARMACY ADDITIVE SYRINGE SETCutter Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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