PLM SENSOR, MODEL PLM1— 510(k) K940014

Name: FDA 510(k) clearance K940014
Creator: U.S. Food and Drug Administration
Published: 1994-11-10

Substantially Equivalent - Subject to Tracking Reg.

Pro-Tech, Inc.

FDA 510(k) clearance K940014 for PLM SENSOR, MODEL PLM1, Substantially Equivalent - Subject to Tracking Reg. on 1994-11-10. Applicant: Pro-Tech, Inc.. Device class: 2.

Clearance details

Applicant: Pro-Tech, Inc.
Product code: Code BZQ
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 1994-01-04
Decision date: 1994-11-10
Decision: Substantially Equivalent - Subject to Tracking Reg.
Clearance type: Traditional
Location: Woodinville, WA, US

Download summary PDF View on FDA.gov ↗

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