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FDA 510(k)

HYDRON WOUND DRESSING FAST SEAT KIT

K-Number: K832699 · 1984-04-27

Decision Date1984-04-27
Product CodeFRO
DecisionSubstantially Equivalent

Device Summary

HYDRON WOUND DRESSING FAST SEAT KIT is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1984-04-27 under 510(k) number K832699. 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 HYDRON WOUND DRESSING FAST SEAT KIT?

HYDRON WOUND DRESSING FAST SEAT KIT is a medical device that received FDA 510(k) clearance on 1984-04-27. The listed applicant is National Patent Development Corp.. The 510(k) number is K832699.

When did HYDRON WOUND DRESSING FAST SEAT KIT receive FDA 510(k) clearance?

HYDRON WOUND DRESSING FAST SEAT KIT received FDA 510(k) clearance on 1984-04-27, under 510(k) number K832699.

Who is the listed applicant for HYDRON WOUND DRESSING FAST SEAT KIT?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRON WOUND DRESSING FAST SEAT KIT?

The FDA product code for HYDRON WOUND DRESSING FAST SEAT KIT 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 National Patent Development Corp. 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 34 devices →

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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