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FDA 510(k)

CRYOPRESS

K-Number: K951769 · 1995-10-16

ApplicantGrimm Scientific Industries, Inc.
Decision Date1995-10-16
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CRYOPRESS is the device name listed in this FDA 510(k) record. The listed applicant is Grimm Scientific Industries, Inc.. It received FDA 510(k) clearance on 1995-10-16 under 510(k) number K951769. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRYOPRESS?

CRYOPRESS is a medical device that received FDA 510(k) clearance on 1995-10-16. The listed applicant is Grimm Scientific Industries, Inc.. The 510(k) number is K951769.

When did CRYOPRESS receive FDA 510(k) clearance?

CRYOPRESS received FDA 510(k) clearance on 1995-10-16, under 510(k) number K951769.

Who is the listed applicant for CRYOPRESS?

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

What is the FDA product code for CRYOPRESS?

The FDA product code for CRYOPRESS is IRP.

Related Clinical Trials

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Other records listing Grimm Scientific Industries, 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.

K864721CRYOTHERMK842423PARA THERM BATH

Related Devices (Code: IRP)

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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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