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FDA 510(k)

TUMBLER, GENERAL MEDICAL MEDI-PAK

K-Number: K760491 · 1976-09-15

ApplicantLandmark Plastics
Decision Date1976-09-15
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUMBLER, GENERAL MEDICAL MEDI-PAK is the device name listed in this FDA 510(k) record. The listed applicant is Landmark Plastics. It received FDA 510(k) clearance on 1976-09-15 under 510(k) number K760491. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUMBLER, GENERAL MEDICAL MEDI-PAK?

TUMBLER, GENERAL MEDICAL MEDI-PAK is a medical device that received FDA 510(k) clearance on 1976-09-15. The listed applicant is Landmark Plastics. The 510(k) number is K760491.

When did TUMBLER, GENERAL MEDICAL MEDI-PAK receive FDA 510(k) clearance?

TUMBLER, GENERAL MEDICAL MEDI-PAK received FDA 510(k) clearance on 1976-09-15, under 510(k) number K760491.

Who is the listed applicant for TUMBLER, GENERAL MEDICAL MEDI-PAK?

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

What is the FDA product code for TUMBLER, GENERAL MEDICAL MEDI-PAK?

The FDA product code for TUMBLER, GENERAL MEDICAL MEDI-PAK is LDR.

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Other records listing Landmark Plastics 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.

K760548CARAFE AND LINERK760493DISH, SOAPK760490BEDPAN, GENERAL MEDICAL MEDI-PAKK760494BASIN, ROUND WASHK760492BASIN, LARGE OR SMALLK760496CUP, DISPOSABLE SPECIMEN

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Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.

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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