MEDSHIELD/AEROCHAMBER— 510(k) K961455

Substantially Equivalent

Diemolding Corp.

FDA 510(k) clearance K961455 for MEDSHIELD/AEROCHAMBER, Substantially Equivalent on 1996-07-25. Applicant: Diemolding Corp.. Device class: 1.

Clearance details

Applicant: Diemolding Corp.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1996-04-16
Decision date: 1996-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

Download summary PDF View on FDA.gov ↗

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K900754 — RESPIREX 21990-03-15
K893791 — BREATHING MOUTHPIECE1989-06-23

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