MONITOR, PULSE WAVE VELOCITY P607— 510(k) K770330

Substantially Equivalent

Cyborg Corp.

FDA 510(k) clearance K770330 for MONITOR, PULSE WAVE VELOCITY P607, Substantially Equivalent on 1977-02-24. Applicant: Cyborg Corp.. Device class: 2.

Clearance details

Applicant: Cyborg Corp.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1977-02-17
Decision date: 1977-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.