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FDA 510(k)

SHAVE PREP KIT

K-Number: K945481 · 1994-12-23

Decision Date1994-12-23
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

SHAVE PREP KIT is the device name listed in this FDA 510(k) record. The listed applicant is Harding Industries, Inc.. It received FDA 510(k) clearance on 1994-12-23 under 510(k) number K945481. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SHAVE PREP KIT?

SHAVE PREP KIT is a medical device that received FDA 510(k) clearance on 1994-12-23. The listed applicant is Harding Industries, Inc.. The 510(k) number is K945481.

When did SHAVE PREP KIT receive FDA 510(k) clearance?

SHAVE PREP KIT received FDA 510(k) clearance on 1994-12-23, under 510(k) number K945481.

Who is the listed applicant for SHAVE PREP KIT?

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

What is the FDA product code for SHAVE PREP KIT?

The FDA product code for SHAVE PREP KIT is LRO.

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 Harding Industries, 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: LRO)

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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