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FDA 510(k)

DOSERIGHT

K-Number: K012238 · 2001-10-01

ApplicantPhilips Medical Systems North America Co.
Decision Date2001-10-01
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DOSERIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America Co.. It received FDA 510(k) clearance on 2001-10-01 under 510(k) number K012238. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSERIGHT?

DOSERIGHT is a medical device that received FDA 510(k) clearance on 2001-10-01. The listed applicant is Philips Medical Systems North America Co.. The 510(k) number is K012238.

When did DOSERIGHT receive FDA 510(k) clearance?

DOSERIGHT received FDA 510(k) clearance on 2001-10-01, under 510(k) number K012238.

Who is the listed applicant for DOSERIGHT?

The FDA 510(k) record lists Philips Medical Systems North America Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DOSERIGHT?

The FDA product code for DOSERIGHT is JAK.

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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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