STRYKER PRESSURE MONITOR SYSTEM— 510(k) K883485

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K883485 for STRYKER PRESSURE MONITOR SYSTEM, Substantially Equivalent on 1988-09-13. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code FTY
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-08-16
Decision date: 1988-09-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, 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.