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FDA 510(k)

ORAL/ENTERAL SYRINGES

K-Number: K100099 · 2010-06-14

ApplicantPhilips Children'S Medical Ventures
Decision Date2010-06-14
Product CodeFPD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ORAL/ENTERAL SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Philips Children'S Medical Ventures. It received FDA 510(k) clearance on 2010-06-14 under 510(k) number K100099. The device is classified under product code FPD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORAL/ENTERAL SYRINGES?

ORAL/ENTERAL SYRINGES is a medical device that received FDA 510(k) clearance on 2010-06-14. The listed applicant is Philips Children'S Medical Ventures. The 510(k) number is K100099.

When did ORAL/ENTERAL SYRINGES receive FDA 510(k) clearance?

ORAL/ENTERAL SYRINGES received FDA 510(k) clearance on 2010-06-14, under 510(k) number K100099.

Who is the listed applicant for ORAL/ENTERAL SYRINGES?

The FDA 510(k) record lists Philips Children'S Medical Ventures as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORAL/ENTERAL SYRINGES?

The FDA product code for ORAL/ENTERAL SYRINGES is FPD.

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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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