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FDA 510(k)

COMPARTMENT SYNDROME PRESSURE MONITOR SYS

K-Number: K844214 · 1985-04-04

ApplicantStryker Corp.
Decision Date1985-04-04
Product CodeLXC
DecisionSubstantially Equivalent

Device Summary

COMPARTMENT SYNDROME PRESSURE MONITOR SYS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1985-04-04 under 510(k) number K844214. The device is classified under product code LXC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPARTMENT SYNDROME PRESSURE MONITOR SYS?

COMPARTMENT SYNDROME PRESSURE MONITOR SYS is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Stryker Corp.. The 510(k) number is K844214.

When did COMPARTMENT SYNDROME PRESSURE MONITOR SYS receive FDA 510(k) clearance?

COMPARTMENT SYNDROME PRESSURE MONITOR SYS received FDA 510(k) clearance on 1985-04-04, under 510(k) number K844214.

Who is the listed applicant for COMPARTMENT SYNDROME PRESSURE MONITOR SYS?

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 COMPARTMENT SYNDROME PRESSURE MONITOR SYS?

The FDA product code for COMPARTMENT SYNDROME PRESSURE MONITOR SYS is LXC.

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Other records listing Stryker Corp. as applicant

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Related Devices (Code: LXC)

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.

K251900MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K242997MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K223509Compremium Compartment Compressibility Monitoring System (CPM#1)Compremium AGK220952MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K210525MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K202635MY01 Continuous Compartmental Pressure MonitorMY01, Inc.

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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