TUBE-TITLE— 510(k) K833361

Substantially Equivalent

Sontek Industries, Inc.

FDA 510(k) clearance K833361 for TUBE-TITLE, Substantially Equivalent on 1983-11-03. Applicant: Sontek Industries, Inc.. Device class: 1.

Clearance details

Applicant: Sontek Industries, Inc.
Product code: Code JAY
Device class: Class 1
Regulation: 21 CFR 868.5280
Advisory panel: Anesthesiology
Date received: 1983-09-27
Decision date: 1983-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAY

K944988 — CUSTOM MEDICAL SUSPENSION STRAP1995-01-27
K873491 — BLOCK, BITE, INTUBATION1987-10-20
K860583 — DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 13151986-02-21
K850924 — JEE FRAME (VENTILATOR CIRCUIT SUPPORT)1985-07-19
K850309 — COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCK1985-02-14

More clearances from Sontek Industries, Inc.

K833372 — BODIA TRACH-SAF DOUBLE SWIVEL1983-11-03
K833373 — BODIA BRONCH-SAF DOUBLE SWIVEL1983-11-03
K833374 — BITE-BLOCK1983-11-03
K813324 — BODAI SWIVEL Y1981-12-29
K812720 — BODAI PATIENT COMMUNICATOR1981-11-05

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