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FDA 510(k)

CRYOBIOLOGICAL FREEZER

K-Number: K881465 · 1988-04-21

ApplicantCryodyne Technologies, Inc.
Decision Date1988-04-21
Product CodeKSP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CRYOBIOLOGICAL FREEZER is the device name listed in this FDA 510(k) record. The listed applicant is Cryodyne Technologies, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881465. The device is classified under product code KSP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOBIOLOGICAL FREEZER?

CRYOBIOLOGICAL FREEZER is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Cryodyne Technologies, Inc.. The 510(k) number is K881465.

When did CRYOBIOLOGICAL FREEZER receive FDA 510(k) clearance?

CRYOBIOLOGICAL FREEZER received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881465.

Who is the listed applicant for CRYOBIOLOGICAL FREEZER?

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

What is the FDA product code for CRYOBIOLOGICAL FREEZER?

The FDA product code for CRYOBIOLOGICAL FREEZER is KSP.

Related Clinical Trials

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Other records listing Cryodyne Technologies, 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.

K926464L.C.S.3000K932520CALIBRATION GASK881467MICROSCOPE STAGE HEATERK881466CELL-CULTURE SHAKERK860738CTC 30, 40, 1 LIQUID OXYGEN LITERS

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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