SENSOCOR TM R-TEST 24OXL— 510(k) K894234

Substantially Equivalent

Sensocor

FDA 510(k) clearance K894234 for SENSOCOR TM R-TEST 24OXL, Substantially Equivalent on 1989-08-03. Applicant: Sensocor. Device class: 2.

Clearance details

Applicant: Sensocor
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1989-06-20
Decision date: 1989-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pompano Beach, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.