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FDA 510(k)

BEESON AUTOMADDAK FEEDER

K-Number: K770169 · 1977-01-28

Decision Date1977-01-28
Product CodeILC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BEESON AUTOMADDAK FEEDER is the device name listed in this FDA 510(k) record. The listed applicant is Techhnilab Instruments, Inc.. It received FDA 510(k) clearance on 1977-01-28 under 510(k) number K770169. The device is classified under product code ILC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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