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FDA 510(k)

KIT, PREP SHAVE

K-Number: K760052 · 1976-07-16

ApplicantM-C Ind., Inc.
Decision Date1976-07-16
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KIT, PREP SHAVE is the device name listed in this FDA 510(k) record. The listed applicant is M-C Ind., Inc.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760052. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIT, PREP SHAVE?

KIT, PREP SHAVE is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is M-C Ind., Inc.. The 510(k) number is K760052.

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

KIT, PREP SHAVE received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760052.

Who is the listed applicant for KIT, PREP SHAVE?

The FDA 510(k) record lists M-C Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIT, PREP SHAVE?

The FDA product code for KIT, PREP SHAVE is LDQ.

Related Clinical Trials

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Other records listing M-C Ind., 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.

K760047TRAY, BLADDER IRRIGATIONK760048TRAY, URETHRAL CATHETERIZATIONK760051TRAY, SUTURE REMOVAL

Related Devices (Code: LDQ)

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.

K993797EC-7701 FLUID WARMING CABINETEnthermics Medical Systems, Inc.K992258HOT SHOT FLUID WARMER IV FLUIDSInfra-Med Technologies, Inc.K981032PIV SYSTEMMedical Solutions, Inc.K973747CONTROLLED TEMPERATURE CABINET SYSTEMSmithK955661ACU-HALTGlederer & Co., Inc.K955776ACU-LABGlederer & Co., Inc.

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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