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FDA 510(k)

REAVILLMED PRESSURE MONITORING SYSTEM AND PICC

K-Number: K101189 · 2010-12-22

ApplicantReavillmed
Decision Date2010-12-22
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REAVILLMED PRESSURE MONITORING SYSTEM AND PICC is the device name listed in this FDA 510(k) record. The listed applicant is Reavillmed. It received FDA 510(k) clearance on 2010-12-22 under 510(k) number K101189. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAVILLMED PRESSURE MONITORING SYSTEM AND PICC?

REAVILLMED PRESSURE MONITORING SYSTEM AND PICC is a medical device that received FDA 510(k) clearance on 2010-12-22. The listed applicant is Reavillmed. The 510(k) number is K101189.

When did REAVILLMED PRESSURE MONITORING SYSTEM AND PICC receive FDA 510(k) clearance?

REAVILLMED PRESSURE MONITORING SYSTEM AND PICC received FDA 510(k) clearance on 2010-12-22, under 510(k) number K101189.

Who is the listed applicant for REAVILLMED PRESSURE MONITORING SYSTEM AND PICC?

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

What is the FDA product code for REAVILLMED PRESSURE MONITORING SYSTEM AND PICC?

The FDA product code for REAVILLMED PRESSURE MONITORING SYSTEM AND PICC is DRS.

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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.

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