BEESON AUTOMADDAK FEEDER
K-Number: K770169 · 1977-01-28
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Device Summary
Frequently Asked Questions
What is the BEESON AUTOMADDAK FEEDER?
BEESON AUTOMADDAK FEEDER is a medical device that received FDA 510(k) clearance on 1977-01-28. The listed applicant is Techhnilab Instruments, Inc.. The 510(k) number is K770169.
When did BEESON AUTOMADDAK FEEDER receive FDA 510(k) clearance?
BEESON AUTOMADDAK FEEDER received FDA 510(k) clearance on 1977-01-28, under 510(k) number K770169.
Who is the listed applicant for BEESON AUTOMADDAK FEEDER?
The FDA 510(k) record lists Techhnilab Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEESON AUTOMADDAK FEEDER?
The FDA product code for BEESON AUTOMADDAK FEEDER is ILC.
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 Techhnilab Instruments, Inc. 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: ILC)
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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