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FDA 510(k)

DEEP FREEZE SYSTEM (DFS-30)

K-Number: K760953 · 1976-11-16

Decision Date1976-11-16
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEEP FREEZE SYSTEM (DFS-30) is the device name listed in this FDA 510(k) record. The listed applicant is Spembly Medical , Ltd.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760953. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 17 devices →

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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