VISER PENILE TUMESCENCE MONITOR— 510(k) K991479

Name: FDA 510(k) clearance K991479
Creator: U.S. Food and Drug Administration
Published: 1999-07-07

Substantially Equivalent

Laborie Medical Tech Corp.

FDA 510(k) clearance K991479 for VISER PENILE TUMESCENCE MONITOR, Substantially Equivalent on 1999-07-07. Applicant: Laborie Medical Tech Corp.. Device class: Unclassified.

Clearance details

Applicant: Laborie Medical Tech Corp.
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1999-04-28
Decision date: 1999-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Williston, VT, US

Download summary PDF View on FDA.gov ↗

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