GENERAL ANESTHESIA SYSTEM— 510(k) K944949

Unknown

Vital Signs, Inc.

FDA 510(k) clearance K944949 for GENERAL ANESTHESIA SYSTEM, Unknown on 1994-11-14. Applicant: Vital Signs, Inc.. Device class: 1.

Clearance details

Applicant: Vital Signs, Inc.
Product code: Code BTK
Device class: Class 1
Regulation: 21 CFR 868.5560
Advisory panel: Anesthesiology
Date received: 1994-10-07
Decision date: 1994-11-14
Decision: Unknown
Clearance type: Traditional
Location: Totowa, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BTK

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K854537 — HEADSTRAP1985-12-03
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K831008 — HEAD STRAP1983-05-09
K810991 — HEADSTRAP1981-04-29

More clearances from Vital Signs, Inc.

K112902 — ENFLOW IV FLUID WARMER2012-03-14
K041309 — IMASK TM2004-06-30
K030985 — BREAS PV 10I CPAP SYSTEM, MODEL PV 10I2003-10-15
K022402 — DISPOSABLE PRESSURE MANOMETER2002-08-22
K021315 — SURE-LOK2002-08-21

Recalls naming K944949

K-number listed on FDA's recall record

Z-0407-2013 — Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperatureClass II·Terminated·Vital Signs Colorado Inc.·20120817

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K944949.

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