DEEP FREEZE SYSTEM (DFS-30)
K-Number: K760953 · 1976-11-16
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Device Summary
Frequently Asked Questions
What is the DEEP FREEZE SYSTEM (DFS-30)?
DEEP FREEZE SYSTEM (DFS-30) is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Spembly Medical , Ltd.. The 510(k) number is K760953.
When did DEEP FREEZE SYSTEM (DFS-30) receive FDA 510(k) clearance?
DEEP FREEZE SYSTEM (DFS-30) received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760953.
Who is the listed applicant for DEEP FREEZE SYSTEM (DFS-30)?
The FDA 510(k) record lists Spembly Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEEP FREEZE SYSTEM (DFS-30)?
The FDA product code for DEEP FREEZE SYSTEM (DFS-30) is GEH.
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 Spembly Medical , Ltd. 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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