LEVERS, DOOR KNOB, BK-6395
K-Number: K760294 · 1976-09-08
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement