SENSOCOR(TM) R-TEST 240 XL— 510(k) K881772

Substantially Equivalent

Sensormedix, Inc.

FDA 510(k) clearance K881772 for SENSOCOR(TM) R-TEST 240 XL, Substantially Equivalent on 1988-11-09. Applicant: Sensormedix, Inc.. Device class: 2.

Clearance details

Applicant: Sensormedix, Inc.
Product code: Code DXH
Device class: Class 2
Regulation: 21 CFR 870.2920
Advisory panel: Cardiovascular
Date received: 1988-04-26
Decision date: 1988-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Lauderdale, FL, US

Download summary PDF View on FDA.gov ↗

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