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FDA 510(k)

ACCUTAPE 24

K-Number: K760508 · 1976-08-30

ApplicantMedcraft Corp.
Decision Date1976-08-30
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ACCUTAPE 24 is the device name listed in this FDA 510(k) record. The listed applicant is Medcraft Corp.. It received FDA 510(k) clearance on 1976-08-30 under 510(k) number K760508. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUTAPE 24?

ACCUTAPE 24 is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is Medcraft Corp.. The 510(k) number is K760508.

When did ACCUTAPE 24 receive FDA 510(k) clearance?

ACCUTAPE 24 received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760508.

Who is the listed applicant for ACCUTAPE 24?

The FDA 510(k) record lists Medcraft Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCUTAPE 24?

The FDA product code for ACCUTAPE 24 is DSH.

Related Clinical Trials

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Other records listing Medcraft Corp. 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.

K860467ELECTROSHOCK UNIT NEUROLOGY MODEL B-25K791795COMP-ACT IVK760510MONITORING SYSTEM, REHABILITATIONK760509TREADMILL, DIAGNOSTIC

Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., Ltd.

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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