NONINVASIVE TEMPORARY PACEMAKER— 510(k) K822246

Name: FDA 510(k) clearance K822246
Creator: U.S. Food and Drug Administration
Published: 1982-08-06

Substantially Equivalent

Ross Research, Inc.

FDA 510(k) clearance K822246 for NONINVASIVE TEMPORARY PACEMAKER, Substantially Equivalent on 1982-08-06. Applicant: Ross Research, Inc.. Device class: 2.

Clearance details

Applicant: Ross Research, Inc.
Product code: Code DRO
Device class: Class 2
Regulation: 21 CFR 870.5550
Advisory panel: Cardiovascular
Date received: 1982-07-29
Decision date: 1982-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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