FDA 510(k)

ARP RX100

K-Number: K093259 · 2009-12-17

Decision Date2009-12-17

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

ARP RX100 is the device name listed in this FDA 510(k) record. The listed applicant is Arp Manufacturing, Inc.. It received FDA 510(k) clearance on 2009-12-17 under 510(k) number K093259. 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 ARP RX100?

ARP RX100 is a medical device that received FDA 510(k) clearance on 2009-12-17. The listed applicant is Arp Manufacturing, Inc.. The 510(k) number is K093259.

When did ARP RX100 receive FDA 510(k) clearance?

ARP RX100 received FDA 510(k) clearance on 2009-12-17, under 510(k) number K093259.

Who is the listed applicant for ARP RX100?

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

What is the FDA product code for ARP RX100?

The FDA product code for ARP RX100 is IPF.

Other records listing Arp Manufacturing, 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.

K093999ARP POV SPORT

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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.