FDA 510(k)

CONVERTORS PRIMARY WOUND DRESSING II

K-Number: K822990 · 1983-04-12

Decision Date1983-04-12

Product CodeFRO

DecisionSubstantially Equivalent

Device Summary

CONVERTORS PRIMARY WOUND DRESSING II is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K822990. 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 CONVERTORS PRIMARY WOUND DRESSING II?

CONVERTORS PRIMARY WOUND DRESSING II is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K822990.

When did CONVERTORS PRIMARY WOUND DRESSING II receive FDA 510(k) clearance?

CONVERTORS PRIMARY WOUND DRESSING II received FDA 510(k) clearance on 1983-04-12, under 510(k) number K822990.

Who is the listed applicant for CONVERTORS PRIMARY WOUND DRESSING II?

The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVERTORS PRIMARY WOUND DRESSING II?

The FDA product code for CONVERTORS PRIMARY WOUND DRESSING II is FRO. This falls under the Anesthesiology category.

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Other records listing American Hospital Supply Corp. as applicant

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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.