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FDA 510(k)

MICROSCOPE STAGE HEATER

K-Number: K881467 · 1988-04-18

ApplicantCryodyne Technologies, Inc.
Decision Date1988-04-18
Product CodeKEJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MICROSCOPE STAGE HEATER 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 1988-04-18 under 510(k) number K881467. The device is classified under product code KEJ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCOPE STAGE HEATER?

MICROSCOPE STAGE HEATER is a medical device that received FDA 510(k) clearance on 1988-04-18. The listed applicant is Cryodyne Technologies, Inc.. The 510(k) number is K881467.

When did MICROSCOPE STAGE HEATER receive FDA 510(k) clearance?

MICROSCOPE STAGE HEATER received FDA 510(k) clearance on 1988-04-18, under 510(k) number K881467.

Who is the listed applicant for MICROSCOPE STAGE HEATER?

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 MICROSCOPE STAGE HEATER?

The FDA product code for MICROSCOPE STAGE HEATER is KEJ.

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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 GASK881465CRYOBIOLOGICAL FREEZERK881466CELL-CULTURE SHAKERK860738CTC 30, 40, 1 LIQUID OXYGEN LITERS

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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