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FDA 510(k)

HISTOFREEZER

K-Number: K931299 · 1993-08-11

ApplicantSolarcare Technologies Corp,Inc.
Decision Date1993-08-11
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HISTOFREEZER is the device name listed in this FDA 510(k) record. The listed applicant is Solarcare Technologies Corp,Inc.. It received FDA 510(k) clearance on 1993-08-11 under 510(k) number K931299. 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 HISTOFREEZER?

HISTOFREEZER is a medical device that received FDA 510(k) clearance on 1993-08-11. The listed applicant is Solarcare Technologies Corp,Inc.. The 510(k) number is K931299.

When did HISTOFREEZER receive FDA 510(k) clearance?

HISTOFREEZER received FDA 510(k) clearance on 1993-08-11, under 510(k) number K931299.

Who is the listed applicant for HISTOFREEZER?

The FDA 510(k) record lists Solarcare Technologies Corp,Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HISTOFREEZER?

The FDA product code for HISTOFREEZER is GEH.

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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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