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FDA 510(k)

ACE INTRA COMPARTMENTAL PRESSURE MONITOR

K-Number: K873684 · 1988-01-20

ApplicantAce Medical Co.
Decision Date1988-01-20
Product CodeLXC
DecisionSubstantially Equivalent

Device Summary

ACE INTRA COMPARTMENTAL PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Ace Medical Co.. It received FDA 510(k) clearance on 1988-01-20 under 510(k) number K873684. The device is classified under product code LXC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE INTRA COMPARTMENTAL PRESSURE MONITOR?

ACE INTRA COMPARTMENTAL PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Ace Medical Co.. The 510(k) number is K873684.

When did ACE INTRA COMPARTMENTAL PRESSURE MONITOR receive FDA 510(k) clearance?

ACE INTRA COMPARTMENTAL PRESSURE MONITOR received FDA 510(k) clearance on 1988-01-20, under 510(k) number K873684.

Who is the listed applicant for ACE INTRA COMPARTMENTAL PRESSURE MONITOR?

The FDA 510(k) record lists Ace Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACE INTRA COMPARTMENTAL PRESSURE MONITOR?

The FDA product code for ACE INTRA COMPARTMENTAL PRESSURE MONITOR is LXC.

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Other records listing Ace Medical Co. 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.

K972183DEPUY ACE A.I.M. TITANIUM TIBIAL NAILK955472ACE HUMERUS & RADIUS PLATESK955388ACE-DUPONT COMPOSITE RINGSK9544856.5MM SOLID CANCELLOUS BONE SCREWK954069ACE CERVICAL TRACTION HALOZS, TONGS & PINSK950618ACE SUPRACONDYLAR PLATE

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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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