Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CS-76 AND/OR CRYOCARE I

K-Number: K760742 · 1976-11-03

Decision Date1976-11-03
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CS-76 AND/OR CRYOCARE I is the device name listed in this FDA 510(k) record. The listed applicant is Frigitronics of Connecticut, Inc.. It received FDA 510(k) clearance on 1976-11-03 under 510(k) number K760742. 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 CS-76 AND/OR CRYOCARE I?

CS-76 AND/OR CRYOCARE I is a medical device that received FDA 510(k) clearance on 1976-11-03. The listed applicant is Frigitronics of Connecticut, Inc.. The 510(k) number is K760742.

When did CS-76 AND/OR CRYOCARE I receive FDA 510(k) clearance?

CS-76 AND/OR CRYOCARE I received FDA 510(k) clearance on 1976-11-03, under 510(k) number K760742.

Who is the listed applicant for CS-76 AND/OR CRYOCARE I?

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

What is the FDA product code for CS-76 AND/OR CRYOCARE I?

The FDA product code for CS-76 AND/OR CRYOCARE I 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 Frigitronics of Connecticut, 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.

View all 9 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.

↑