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FDA 510(k)

CURITY TRANSPARENT FILM DRESSING

K-Number: K822424 · 1982-12-17

Decision Date1982-12-17
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

CURITY TRANSPARENT FILM DRESSING 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 1982-12-17 under 510(k) number K822424. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY TRANSPARENT FILM DRESSING?

CURITY TRANSPARENT FILM DRESSING is a medical device that received FDA 510(k) clearance on 1982-12-17. The listed applicant is The Kendal Co.. The 510(k) number is K822424.

When did CURITY TRANSPARENT FILM DRESSING receive FDA 510(k) clearance?

CURITY TRANSPARENT FILM DRESSING received FDA 510(k) clearance on 1982-12-17, under 510(k) number K822424.

Who is the listed applicant for CURITY TRANSPARENT FILM DRESSING?

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 TRANSPARENT FILM DRESSING?

The FDA product code for CURITY TRANSPARENT FILM DRESSING is FRO. This falls under the Anesthesiology category.

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: FRO)

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

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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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