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FDA 510(k)

IAMIN WET DRESSING (COPPER-SALINE)

K-Number: K964468 · 1997-02-03

ApplicantProcyte Corp.
Decision Date1997-02-03
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

IAMIN WET DRESSING (COPPER-SALINE) is the device name listed in this FDA 510(k) record. The listed applicant is Procyte Corp.. It received FDA 510(k) clearance on 1997-02-03 under 510(k) number K964468. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IAMIN WET DRESSING (COPPER-SALINE)?

IAMIN WET DRESSING (COPPER-SALINE) is a medical device that received FDA 510(k) clearance on 1997-02-03. The listed applicant is Procyte Corp.. The 510(k) number is K964468.

When did IAMIN WET DRESSING (COPPER-SALINE) receive FDA 510(k) clearance?

IAMIN WET DRESSING (COPPER-SALINE) received FDA 510(k) clearance on 1997-02-03, under 510(k) number K964468.

Who is the listed applicant for IAMIN WET DRESSING (COPPER-SALINE)?

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

What is the FDA product code for IAMIN WET DRESSING (COPPER-SALINE)?

The FDA product code for IAMIN WET DRESSING (COPPER-SALINE) is MGQ.

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Other records listing Procyte 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.

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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.

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