STRYKER PRESSURE MONITOR SYSTEM
K-Number: K883485 · 1988-09-13
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Device Summary
Frequently Asked Questions
What is the STRYKER PRESSURE MONITOR SYSTEM?
STRYKER PRESSURE MONITOR SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-13. The listed applicant is Stryker Corp.. The 510(k) number is K883485.
When did STRYKER PRESSURE MONITOR SYSTEM receive FDA 510(k) clearance?
STRYKER PRESSURE MONITOR SYSTEM received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883485.
Who is the listed applicant for STRYKER PRESSURE MONITOR SYSTEM?
The FDA 510(k) record lists Stryker Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER PRESSURE MONITOR SYSTEM?
The FDA product code for STRYKER PRESSURE MONITOR SYSTEM is FTY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Stryker Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FTY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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