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FDA 510(k)

DISPOSE-A-SHEET

K-Number: K933636 · 1994-01-26

Decision Date1994-01-26
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSE-A-SHEET is the device name listed in this FDA 510(k) record. The listed applicant is Belmac Healthcare Corp.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K933636. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSE-A-SHEET?

DISPOSE-A-SHEET is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Belmac Healthcare Corp.. The 510(k) number is K933636.

When did DISPOSE-A-SHEET receive FDA 510(k) clearance?

DISPOSE-A-SHEET received FDA 510(k) clearance on 1994-01-26, under 510(k) number K933636.

Who is the listed applicant for DISPOSE-A-SHEET?

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

What is the FDA product code for DISPOSE-A-SHEET?

The FDA product code for DISPOSE-A-SHEET is KME.

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.

Related Devices (Code: KME)

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

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

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