PRESSURE MONITOR, MODEL 212— 510(k) K790302

Substantially Equivalent

Zatek

FDA 510(k) clearance K790302 for PRESSURE MONITOR, MODEL 212, Substantially Equivalent on 1979-03-21. Applicant: Zatek. Device class: 1.

Clearance details

Applicant: Zatek
Product code: Code HRW
Device class: Class 1
Regulation: 21 CFR 888.1250
Advisory panel: Orthopedic
Date received: 1979-02-13
Decision date: 1979-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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