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FDA 510(k)

CURITY PERINEAL COLD PACK

K-Number: K810693 · 1981-03-26

Decision Date1981-03-26
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CURITY PERINEAL COLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1981-03-26 under 510(k) number K810693. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY PERINEAL COLD PACK?

CURITY PERINEAL COLD PACK is a medical device that received FDA 510(k) clearance on 1981-03-26. The listed applicant is The Kendal Co.. The 510(k) number is K810693.

When did CURITY PERINEAL COLD PACK receive FDA 510(k) clearance?

CURITY PERINEAL COLD PACK received FDA 510(k) clearance on 1981-03-26, under 510(k) number K810693.

Who is the listed applicant for CURITY PERINEAL COLD PACK?

The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY PERINEAL COLD PACK?

The FDA product code for CURITY PERINEAL COLD PACK is IMD.

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 The Kendal Co. 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.

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Related Devices (Code: IMD)

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.

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