PRESSURE ALARM— 510(k) K782174

Name: FDA 510(k) clearance K782174
Creator: U.S. Food and Drug Administration
Published: 1979-01-22

Substantially Equivalent

Thompson Respiration Products, Inc.

FDA 510(k) clearance K782174 for PRESSURE ALARM, Substantially Equivalent on 1979-01-22. Applicant: Thompson Respiration Products, Inc.. Device class: 2.

Clearance details

Applicant: Thompson Respiration Products, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 1978-12-19
Decision date: 1979-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K822103 — MODEL M3000XA VENTILATOR SPECIFICA1982-07-26
K781158 — ALARM UNIT, BATTERY OPERATED1978-12-18
K781160 — VENTILATOR, MINILUNG1978-12-13
K781159 — VENTILATOR, PRESSURE1978-12-12
K781161 — RESPIRATOR, BANTAM MODEL1978-12-11

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