VACUUM REGULATOR 0-2000 MMHG VR-1000— 510(k) K834224

Name: FDA 510(k) clearance K834224
Creator: U.S. Food and Drug Administration
Published: 1984-02-27

Substantially Equivalent

Trimeter Instrument Corp.

FDA 510(k) clearance K834224 for VACUUM REGULATOR 0-2000 MMHG VR-1000, Substantially Equivalent on 1984-02-27. Applicant: Trimeter Instrument Corp.. Device class: 2.

Clearance details

Applicant: Trimeter Instrument Corp.
Product code: Code KDP
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1983-12-06
Decision date: 1984-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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