AGAR 4000 NEUROMUSCULAR STIMULATOR— 510(k) K882387

Name: FDA 510(k) clearance K882387
Creator: U.S. Food and Drug Administration
Published: 1989-10-16

Substantially Equivalent

Solcoor, Inc.

FDA 510(k) clearance K882387 for AGAR 4000 NEUROMUSCULAR STIMULATOR, Substantially Equivalent on 1989-10-16. Applicant: Solcoor, Inc.. Device class: 2.

Clearance details

Applicant: Solcoor, Inc.
Product code: Code IPF
Device class: Class 2
Regulation: 21 CFR 890.5850
Advisory panel: Physical Medicine
Date received: 1988-06-10
Decision date: 1989-10-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Vienna, VA, US

Download summary PDF View on FDA.gov ↗

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