BOSWORTH CH I
K-Number: K961198 · 1996-05-24
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Device Summary
Frequently Asked Questions
What is the BOSWORTH CH I?
BOSWORTH CH I is a medical device that received FDA 510(k) clearance on 1996-05-24. The listed applicant is Harry J. Bosworth Co.. The 510(k) number is K961198.
When did BOSWORTH CH I receive FDA 510(k) clearance?
BOSWORTH CH I received FDA 510(k) clearance on 1996-05-24, under 510(k) number K961198.
Who is the listed applicant for BOSWORTH CH I?
The FDA 510(k) record lists Harry J. Bosworth Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSWORTH CH I?
The FDA product code for BOSWORTH CH I is EBG.
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 Harry J. Bosworth Co. 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: EBG)
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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