EPI-LOCK WOUND DRESSING— 510(k) K926034

Name: FDA 510(k) clearance K926034
Creator: U.S. Food and Drug Administration
Published: 1993-04-20

Substantially Equivalent

Calgon Vestal Div.

FDA 510(k) clearance K926034 for EPI-LOCK WOUND DRESSING, Substantially Equivalent on 1993-04-20. Applicant: Calgon Vestal Div.. Device class: Unclassified.

Clearance details

Applicant: Calgon Vestal Div.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-12-01
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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K012997 — COLLATEK FOAM2001-10-25
K001508 — LASERSKIN DRESSING2001-07-25
K990079 — FASTSEAL CHEST WOUND DRESSING1999-12-23
K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14

More clearances from Calgon Vestal Div.

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K944494 — ALSA-KLENZ1994-10-19
K944033 — BILL EVANS-KLENZ1994-10-07
K942270 — SAF-GEL HYDRATING DERMAL WOUND DRESSING1994-08-04
K931477 — AMERSE1994-06-17
K931342 — LPH1994-05-26

Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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