FLEXIBLE EXTENDER
K-Number: K902035 · 1990-07-19
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE EXTENDER?
FLEXIBLE EXTENDER is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Beacon Laboratories, Inc.. The 510(k) number is K902035.
When did FLEXIBLE EXTENDER receive FDA 510(k) clearance?
FLEXIBLE EXTENDER received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902035.
Who is the listed applicant for FLEXIBLE EXTENDER?
The FDA 510(k) record lists Beacon Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE EXTENDER?
The FDA product code for 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 Beacon Laboratories, 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.
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