HM-CRYO
K-Number: K940140 · 1994-06-27
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Device Summary
Frequently Asked Questions
What is the HM-CRYO?
HM-CRYO is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Hill-Med, Inc.. The 510(k) number is K940140.
When did HM-CRYO receive FDA 510(k) clearance?
HM-CRYO received FDA 510(k) clearance on 1994-06-27, under 510(k) number K940140.
Who is the listed applicant for HM-CRYO?
The FDA 510(k) record lists Hill-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HM-CRYO?
The FDA product code for HM-CRYO is GEH.
Other records listing Hill-Med, 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: GEH)
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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