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FDA 510(k)

SINGLE-USE MINI-BULLDOG

K-Number: K791098 · 1979-06-22

ApplicantMed General
Decision Date1979-06-22
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SINGLE-USE MINI-BULLDOG is the device name listed in this FDA 510(k) record. The listed applicant is Med General. It received FDA 510(k) clearance on 1979-06-22 under 510(k) number K791098. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE-USE MINI-BULLDOG?

SINGLE-USE MINI-BULLDOG is a medical device that received FDA 510(k) clearance on 1979-06-22. The listed applicant is Med General. The 510(k) number is K791098.

When did SINGLE-USE MINI-BULLDOG receive FDA 510(k) clearance?

SINGLE-USE MINI-BULLDOG received FDA 510(k) clearance on 1979-06-22, under 510(k) number K791098.

Who is the listed applicant for SINGLE-USE MINI-BULLDOG?

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 SINGLE-USE MINI-BULLDOG?

The FDA product code for SINGLE-USE MINI-BULLDOG is DXC.

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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 HESIVEK790763MAXI-VAC TMK790269CEPTOR HESIVEK782006MEDGENERAL SINGLE-USE BULLDOGK781239MYO-STIMK780632MAXICEPTOR

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Related Devices (Code: DXC)

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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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