HYPOGRIP(TM)
K-Number: K924820 · 1993-10-05
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Device Summary
Frequently Asked Questions
What is the HYPOGRIP(TM)?
HYPOGRIP(TM) is a medical device that received FDA 510(k) clearance on 1993-10-05. The listed applicant is Collett Products. The 510(k) number is K924820.
When did HYPOGRIP(TM) receive FDA 510(k) clearance?
HYPOGRIP(TM) received FDA 510(k) clearance on 1993-10-05, under 510(k) number K924820.
Who is the listed applicant for HYPOGRIP(TM)?
The FDA 510(k) record lists Collett Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYPOGRIP(TM)?
The FDA product code for HYPOGRIP(TM) is FMI.
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.
Related Devices (Code: FMI)
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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