MEDGENERAL SINGLE-USE BULLDOG
K-Number: K782006 · 1978-12-15
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Device Summary
Frequently Asked Questions
What is the MEDGENERAL SINGLE-USE BULLDOG?
MEDGENERAL SINGLE-USE BULLDOG is a medical device that received FDA 510(k) clearance on 1978-12-15. The listed applicant is Med General. The 510(k) number is K782006.
When did MEDGENERAL SINGLE-USE BULLDOG receive FDA 510(k) clearance?
MEDGENERAL SINGLE-USE BULLDOG received FDA 510(k) clearance on 1978-12-15, under 510(k) number K782006.
Who is the listed applicant for MEDGENERAL SINGLE-USE 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 MEDGENERAL SINGLE-USE BULLDOG?
The FDA product code for MEDGENERAL SINGLE-USE BULLDOG is GDJ.
Related Clinical Trials
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.
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.
Related Devices (Code: GDJ)
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.
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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