INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR— 510(k) K800179

Name: FDA 510(k) clearance K800179
Creator: U.S. Food and Drug Administration
Published: 1980-02-11

Substantially Equivalent

Sphygmetrics, Inc.

FDA 510(k) clearance K800179 for INFRASONDE AUTO/INFLATOR ELEC. VIBRATOR, Substantially Equivalent on 1980-02-11. Applicant: Sphygmetrics, Inc.. Device class: 2.

Clearance details

Applicant: Sphygmetrics, Inc.
Product code: Code DXW
Device class: Class 2
Regulation: 21 CFR 870.1270
Advisory panel: Cardiovascular
Date received: 1980-01-29
Decision date: 1980-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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