COPOLYESTER FILM DRESSING— 510(k) K893647

Name: FDA 510(k) clearance K893647
Creator: U.S. Food and Drug Administration
Published: 1989-10-16

Substantially Equivalent

Tri-State Hospital Supply Corp.

FDA 510(k) clearance K893647 for COPOLYESTER FILM DRESSING, Substantially Equivalent on 1989-10-16. Applicant: Tri-State Hospital Supply Corp.. Device class: Unclassified.

Clearance details

Applicant: Tri-State Hospital Supply Corp.
Product code: Code KGN
Device class: Unclassified
Advisory panel: Unknown
Date received: 1989-05-15
Decision date: 1989-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Howell, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KGN

view all

K260652 — ColActive Plus2026-09-09
K260711 — Accelagen Plus Surgical Matrix, 1cc (CG-01AP) +4 more2026-08-27
K260596 — Collagen Wound Powder2026-07-02
K260669 — Endoform Dermal Template2026-06-24
K253521 — ECMT-100 WMD2026-06-18

More clearances from Tri-State Hospital Supply Corp.

view all

K080448 — CENTURION PROTECTIVE RESTRAINT, SCR SERIES2008-08-28
K080524 — CENTURION SORBAVIEW OTC2008-04-23
K942353 — CENTURION UMBILICAL CATHETER1995-08-15
K945977 — CENTURION(R) SITE GUARD(R) TRANSPARENT DRESSING/TRANSPAENT FILM DRESSING1995-03-29
K931748 — CENTLURION DISP STERI DENTAL/HYGIENE PACK/TRAYS1994-02-25

Adverse events under product code KGN

product code KGN

Other: 2
Total: 2

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.