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FDA 510(k)

CEPTOR HESIVE

K-Number: K790269 · 1979-02-26

ApplicantMed General
Decision Date1979-02-26
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CEPTOR HESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Med General. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K790269. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEPTOR HESIVE?

CEPTOR HESIVE is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Med General. The 510(k) number is K790269.

When did CEPTOR HESIVE receive FDA 510(k) clearance?

CEPTOR HESIVE received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790269.

Who is the listed applicant for CEPTOR HESIVE?

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

What is the FDA product code for CEPTOR HESIVE?

The FDA product code for CEPTOR HESIVE is GXY.

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Other records listing Med General 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.

K791097CEPTORTRODE WITH CEPTOR HESIVEK791098SINGLE-USE MINI-BULLDOGK790763MAXI-VAC TMK782006MEDGENERAL SINGLE-USE BULLDOGK781239MYO-STIMK780632MAXICEPTOR

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Related Devices (Code: GXY)

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.

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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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