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FDA 510(k)

AMPCO PROCEDURE TRAYS / PACKS

K-Number: K843114 · 1984-08-08

ApplicantAssociated Medical Products Co.
Decision Date1984-08-08
Product Code
DecisionUnknown

Device Summary

AMPCO PROCEDURE TRAYS / PACKS 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 1984-08-08 under 510(k) number K843114. FDA Decision: Unknown.

Frequently Asked Questions

What is the AMPCO PROCEDURE TRAYS / PACKS?

AMPCO PROCEDURE TRAYS / PACKS is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Associated Medical Products Co.. The 510(k) number is K843114.

When did AMPCO PROCEDURE TRAYS / PACKS receive FDA 510(k) clearance?

AMPCO PROCEDURE TRAYS / PACKS received FDA 510(k) clearance on 1984-08-08, under 510(k) number K843114.

Who is the listed applicant for AMPCO PROCEDURE TRAYS / PACKS?

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

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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

View all 29 devices →

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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