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FDA 510(k)

SKIN SCRUB-TRAY

K-Number: K821579 · 1982-07-21

ApplicantAssociated Medical Products Co.
Decision Date1982-07-21
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SKIN SCRUB-TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Associated Medical Products Co.. It received FDA 510(k) clearance on 1982-07-21 under 510(k) number K821579. 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 SKIN SCRUB-TRAY?

SKIN SCRUB-TRAY is a medical device that received FDA 510(k) clearance on 1982-07-21. The listed applicant is Associated Medical Products Co.. The 510(k) number is K821579.

When did SKIN SCRUB-TRAY receive FDA 510(k) clearance?

SKIN SCRUB-TRAY received FDA 510(k) clearance on 1982-07-21, under 510(k) number K821579.

Who is the listed applicant for SKIN SCRUB-TRAY?

The FDA 510(k) record lists Associated Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SKIN SCRUB-TRAY?

The FDA product code for SKIN SCRUB-TRAY is LDR.

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Other records listing Associated Medical Products Co. 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.

K932221NEUROLOGICAL OR CRANI TRAYS (PACKS)K932216C-SECTION, LABOR & DELIVERY TRAYS (PACKS)K930507CUSTOM ORTHOPAEDIC TRAYS (PACKS)K932217MAJOR, MINOR, BASIN TRAYS (PACKS)K932220LAP CHOLY TRAYS (PACKS)K932218CARDIAC CATH OR ANGIOGRAPHIC TRAYS

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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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