DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL— 510(k) K896511

Name: FDA 510(k) clearance K896511
Creator: U.S. Food and Drug Administration
Published: 1989-12-22

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K896511 for DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL, Substantially Equivalent on 1989-12-22. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: 1.

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code KPY
Device class: Class 1
Regulation: 21 CFR 892.6500
Advisory panel: Radiology
Date received: 1989-11-14
Decision date: 1989-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPY

view all

K110900 — DISPOSABLE THYROID COLLAR2011-06-24
K962622 — INTRA-ORAL THERMOPLASTIC SHIELD1996-10-01
K954456 — THERMOPLASTIC SHIELD1995-12-21
K954146 — UTK-DTE AUTILARY SHIELD1995-12-06
K953610 — AUKULYTE1995-09-26

More clearances from E.I. Dupont DE Nemours & Co., Inc.

view all

K951851 — ALLIANCE CYTOMEGALOVIRUS IMMEDIATE EARLY ANTIGEN DIRECT IMMUNOFLUORESCENCE ASSAY1996-07-24
K953724 — CRONEX RADIATION THERAPY CASSETTE1995-09-06
K953725 — CRONEX RADIATION THERAPY VERIFICATION CASSETTE1995-09-06
K951441 — DUPONT ACA DIGOXIN (DGN A) METHOD1995-06-01
K950137 — URINE BARBITURATES SCREEN FLEX(TM) REAGENT CARTRIDGE1995-04-13

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