IAMIN WET DRESSING (COPPER-SALINE)— 510(k) K964468

Substantially Equivalent

Procyte Corp.

FDA 510(k) clearance K964468 for IAMIN WET DRESSING (COPPER-SALINE), Substantially Equivalent on 1997-02-03. Applicant: Procyte Corp.. Device class: Unclassified.

Clearance details

Applicant
Procyte Corp.
Product code
Code MGQ
Device class
Unclassified
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Kirkland, WA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code MGQ

product code MGQ
Death
16
Total
16

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K964468

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K964468.

Data sourced from openFDA. This site is unofficial and independent of the FDA.