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FDA 510(k)

CP SLEEVE AND RIVER SLEEVE

K-Number: K034062 · 2004-01-30

ApplicantCp Medical
Decision Date2004-01-30
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CP SLEEVE AND RIVER SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Cp Medical. It received FDA 510(k) clearance on 2004-01-30 under 510(k) number K034062. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CP SLEEVE AND RIVER SLEEVE?

CP SLEEVE AND RIVER SLEEVE is a medical device that received FDA 510(k) clearance on 2004-01-30. The listed applicant is Cp Medical. The 510(k) number is K034062.

When did CP SLEEVE AND RIVER SLEEVE receive FDA 510(k) clearance?

CP SLEEVE AND RIVER SLEEVE received FDA 510(k) clearance on 2004-01-30, under 510(k) number K034062.

Who is the listed applicant for CP SLEEVE AND RIVER SLEEVE?

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

What is the FDA product code for CP SLEEVE AND RIVER SLEEVE?

The FDA product code for CP SLEEVE AND RIVER SLEEVE is KXK.

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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.

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Other records listing Cp Medical 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.

K094028CP-FIBER (ORTHOFIBER)K072229MONOSWIFTK071550PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERSK060987OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31K041894ORTHOFIBERK024372CP MEDICAL BONE WAX

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Related Devices (Code: KXK)

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.

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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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