FDA 510(k)

PCI 2500

K-Number: K933072 · 1993-10-28

ApplicantPci

Decision Date1993-10-28

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

PCI 2500 is the device name listed in this FDA 510(k) record. The listed applicant is Pci. It received FDA 510(k) clearance on 1993-10-28 under 510(k) number K933072. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PCI 2500?

PCI 2500 is a medical device that received FDA 510(k) clearance on 1993-10-28. The listed applicant is Pci. The 510(k) number is K933072.

When did PCI 2500 receive FDA 510(k) clearance?

PCI 2500 received FDA 510(k) clearance on 1993-10-28, under 510(k) number K933072.

Who is the listed applicant for PCI 2500?

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

What is the FDA product code for PCI 2500?

The FDA product code for PCI 2500 is IPF.

Other records listing Pci 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.

K932610PCI 4000

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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.