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FDA 510(k)

SWR DISPOSABLE PREP RAZOR

K-Number: K810112 · 1981-02-04

Decision Date1981-02-04
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SWR DISPOSABLE PREP RAZOR is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1981-02-04 under 510(k) number K810112. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWR DISPOSABLE PREP RAZOR?

SWR DISPOSABLE PREP RAZOR is a medical device that received FDA 510(k) clearance on 1981-02-04. The listed applicant is G.D. Searle and Co.. The 510(k) number is K810112.

When did SWR DISPOSABLE PREP RAZOR receive FDA 510(k) clearance?

SWR DISPOSABLE PREP RAZOR received FDA 510(k) clearance on 1981-02-04, under 510(k) number K810112.

Who is the listed applicant for SWR DISPOSABLE PREP RAZOR?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SWR DISPOSABLE PREP RAZOR?

The FDA product code for SWR DISPOSABLE PREP RAZOR is KDC.

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 G.D. Searle and 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 56 devices →

Related Devices (Code: KDC)

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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