FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER
K-Number: K924524 · 1993-04-05
Advertisement
Device Summary
Frequently Asked Questions
What is the FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER?
FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER is a medical device that received FDA 510(k) clearance on 1993-04-05. The listed applicant is Valleylab, Inc.. The 510(k) number is K924524.
When did FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER receive FDA 510(k) clearance?
FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER received FDA 510(k) clearance on 1993-04-05, under 510(k) number K924524.
Who is the listed applicant for FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER?
The FDA 510(k) record lists Valleylab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER?
The FDA product code for FORCE GSU(TM) HANDSET W/3 & 6 FLEXIBLE EXTENDER is GEI.
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 Valleylab, 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: GEI)
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