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FDA 510(k)

AMPCO SKIN SCRUB TRAY

K-Number: K802375 · 1980-10-10

Decision Date1980-10-10
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMPCO 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 1980-10-10 under 510(k) number K802375. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPCO SKIN SCRUB TRAY?

AMPCO SKIN SCRUB TRAY is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Associated Medical Products Co.. The 510(k) number is K802375.

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

AMPCO SKIN SCRUB TRAY received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802375.

Who is the listed applicant for AMPCO 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 AMPCO SKIN SCRUB TRAY?

The FDA product code for AMPCO SKIN SCRUB TRAY is FMC.

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.

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.

View all 29 devices →

Related Devices (Code: FMC)

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.

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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