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FDA 510(k)

BIO-GUARD SHAVE PREP TRAY

K-Number: K905003 · 1990-12-28

Decision Date1990-12-28
Product CodeKME
Advisory CommitteeHO
DecisionUnknown

Device Summary

BIO-GUARD SHAVE PREP TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Network Medical Systems, Inc.. It received FDA 510(k) clearance on 1990-12-28 under 510(k) number K905003. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BIO-GUARD SHAVE PREP TRAY?

BIO-GUARD SHAVE PREP TRAY is a medical device that received FDA 510(k) clearance on 1990-12-28. The listed applicant is Network Medical Systems, Inc.. The 510(k) number is K905003.

When did BIO-GUARD SHAVE PREP TRAY receive FDA 510(k) clearance?

BIO-GUARD SHAVE PREP TRAY received FDA 510(k) clearance on 1990-12-28, under 510(k) number K905003.

Who is the listed applicant for BIO-GUARD SHAVE PREP TRAY?

The FDA 510(k) record lists Network Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-GUARD SHAVE PREP TRAY?

The FDA product code for BIO-GUARD SHAVE PREP TRAY 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 Network Medical Systems, Inc. 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.

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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