THE DENVER SPLINT— 510(k) K791053

Substantially Equivalent

Ronald D. Shippert, M.D.

FDA 510(k) clearance K791053 for THE DENVER SPLINT, Substantially Equivalent on 1979-08-16. Applicant: Ronald D. Shippert, M.D.. Device class: 1.

Clearance details

Applicant: Ronald D. Shippert, M.D.
Product code: Code EPP
Device class: Class 1
Regulation: 21 CFR 874.5800
Advisory panel: Ear, Nose, Throat
Date received: 1979-06-06
Decision date: 1979-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EPP

K942158 — AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITS1994-07-29
K942724 — EXTERNAL NASAL SPLINT1994-07-08
K895502 — MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINT1989-12-08
K890599 — HOOD NASAL SPLINT1989-03-17
K882244 — RICHARDS THERMOPLASTIC DORSAL NASAL SPLINT1988-06-23

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