ALARM UNIT, BATTERY OPERATED— 510(k) K781158

Name: FDA 510(k) clearance K781158
Creator: U.S. Food and Drug Administration
Published: 1978-12-18

Substantially Equivalent

Thompson Respiration Products, Inc.

FDA 510(k) clearance K781158 for ALARM UNIT, BATTERY OPERATED, Substantially Equivalent on 1978-12-18. Applicant: Thompson Respiration Products, Inc.. Device class: 2.

Clearance details

Applicant: Thompson Respiration Products, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1978-07-05
Decision date: 1978-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZQ

view all

K253274 — BedDot (G1)2026-06-25
K251326 — Respiration Rate algorithm2026-06-11
K250093 — Linshom Continuous Predictive Respiratory Monitoring System (CPRMS)2025-09-26
K250934 — Respiree Cardio- Respiratory Monitor System2025-08-05
K243183 — RTMsense Respiratory Monitoring System2025-06-27

More clearances from Thompson Respiration Products, Inc.

view all

K822103 — MODEL M3000XA VENTILATOR SPECIFICA1982-07-26
K782174 — PRESSURE ALARM1979-01-22
K781160 — VENTILATOR, MINILUNG1978-12-13
K781159 — VENTILATOR, PRESSURE1978-12-12
K781161 — RESPIRATOR, BANTAM MODEL1978-12-11

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