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FDA 510(k)

LEVERS, DOOR KNOB, BK-6395

K-Number: K760294 · 1976-09-08

Decision Date1976-09-08
Product CodeIKW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LEVERS, DOOR KNOB, BK-6395 is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1976-09-08 under 510(k) number K760294. The device is classified under product code IKW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVERS, DOOR KNOB, BK-6395?

LEVERS, DOOR KNOB, BK-6395 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760294.

When did LEVERS, DOOR KNOB, BK-6395 receive FDA 510(k) clearance?

LEVERS, DOOR KNOB, BK-6395 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760294.

Who is the listed applicant for LEVERS, DOOR KNOB, BK-6395?

The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVERS, DOOR KNOB, BK-6395?

The FDA product code for LEVERS, DOOR KNOB, BK-6395 is IKW.

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 Fred Sammons, 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.

View all 278 devices →

Related Devices (Code: IKW)

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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