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FDA 510(k)

MAR COR SERVICES SEMPER PURE RO MACHINE

K-Number: K003877 · 2001-06-22

Decision Date2001-06-22
Product CodeFIP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAR COR SERVICES SEMPER PURE RO MACHINE is the device name listed in this FDA 510(k) record. The listed applicant is Mar Cor Services, Inc.. It received FDA 510(k) clearance on 2001-06-22 under 510(k) number K003877. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAR COR SERVICES SEMPER PURE RO MACHINE?

MAR COR SERVICES SEMPER PURE RO MACHINE is a medical device that received FDA 510(k) clearance on 2001-06-22. The listed applicant is Mar Cor Services, Inc.. The 510(k) number is K003877.

When did MAR COR SERVICES SEMPER PURE RO MACHINE receive FDA 510(k) clearance?

MAR COR SERVICES SEMPER PURE RO MACHINE received FDA 510(k) clearance on 2001-06-22, under 510(k) number K003877.

Who is the listed applicant for MAR COR SERVICES SEMPER PURE RO MACHINE?

The FDA 510(k) record lists Mar Cor Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAR COR SERVICES SEMPER PURE RO MACHINE?

The FDA product code for MAR COR SERVICES SEMPER PURE RO MACHINE is FIP.

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 Mar Cor Services, Inc. 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: FIP)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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