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FDA 510(k)

CEPTORTRODE WITH CEPTOR HESIVE

K-Number: K791097 · 1979-08-03

ApplicantMed General
Decision Date1979-08-03
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CEPTORTRODE WITH 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 1979-08-03 under 510(k) number K791097. 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 CEPTORTRODE WITH CEPTOR HESIVE?

CEPTORTRODE WITH CEPTOR HESIVE is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Med General. The 510(k) number is K791097.

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

CEPTORTRODE WITH CEPTOR HESIVE received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791097.

Who is the listed applicant for CEPTORTRODE WITH 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 CEPTORTRODE WITH CEPTOR HESIVE?

The FDA product code for CEPTORTRODE WITH 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.

K791098SINGLE-USE MINI-BULLDOGK790763MAXI-VAC TMK790269CEPTOR HESIVEK782006MEDGENERAL 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.

K262654Dexus Prosthetic System (MSL2, MSR2)Zhejiang Qiangnao Technology Co.,LtdK260578Ambu® NeurolineTM Cup MRI/CT (Models 72704/21US, 72704/23US, 72704/25US, 72704/27US) Ambu® NeurolineTM Cup MRI/CT-set (Models 72704/21-1010US, 72704/21-1010US, 72704/23-1010US, 72704/25-1010US, 72704/27-1010US) Ambu® NeurolineTM Cup MRI/CT-mini set (Models 72704/21-0301US, 72704/23-0301US, 72704/25-0301US, 72704/27-0301US)Ambu A/SK261442Charlotte ACC25 Surface Electrode Array; Charlotte ACC25 Reusable Surface Electrode ArrayCadwell Industries, Inc.K261522BioWave BioWrapsBiowave CorporationK253237Elde Medical Electrodes (T5/ 5 cm x 5cm electrode T10/ 5 cm x 10cm electrode)Elde Medikal Sanayi ve Ticaret Anonim SirketiK254183MR Conditional Cup ElectrodesTechnomed Europe

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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