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FDA 510(k)

WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT

K-Number: K844196 · 1984-12-04

Decision Date1984-12-04
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT is the device name listed in this FDA 510(k) record. The listed applicant is Biological & Environmental Control Laboratories. It received FDA 510(k) clearance on 1984-12-04 under 510(k) number K844196. 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 WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT?

WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT is a medical device that received FDA 510(k) clearance on 1984-12-04. The listed applicant is Biological & Environmental Control Laboratories. The 510(k) number is K844196.

When did WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT receive FDA 510(k) clearance?

WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT received FDA 510(k) clearance on 1984-12-04, under 510(k) number K844196.

Who is the listed applicant for WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT?

The FDA 510(k) record lists Biological & Environmental Control Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT?

The FDA product code for WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT 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.

Other records listing Biological & Environmental Control Laboratories 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.

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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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