BODIA BRONCH-SAF DOUBLE SWIVEL— 510(k) K833373

Name: FDA 510(k) clearance K833373
Creator: U.S. Food and Drug Administration
Published: 1983-11-03

Substantially Equivalent

Sontek Industries, Inc.

FDA 510(k) clearance K833373 for BODIA BRONCH-SAF DOUBLE SWIVEL, Substantially Equivalent on 1983-11-03. Applicant: Sontek Industries, Inc.. Device class: 1.

Clearance details

Applicant: Sontek Industries, Inc.
Product code: Code BZA
Device class: Class 1
Regulation: 21 CFR 868.5810
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 ↗

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K833361 — TUBE-TITLE1983-11-03
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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.