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FDA 510(k)

INTERA-SENSATION FAMILY

K-Number: K031815 · 2003-09-10

ApplicantPhilips Medical Systems
Decision Date2003-09-10
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERA-SENSATION FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2003-09-10 under 510(k) number K031815. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERA-SENSATION FAMILY?

INTERA-SENSATION FAMILY is a medical device that received FDA 510(k) clearance on 2003-09-10. The listed applicant is Philips Medical Systems. The 510(k) number is K031815.

When did INTERA-SENSATION FAMILY receive FDA 510(k) clearance?

INTERA-SENSATION FAMILY received FDA 510(k) clearance on 2003-09-10, under 510(k) number K031815.

Who is the listed applicant for INTERA-SENSATION FAMILY?

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

What is the FDA product code for INTERA-SENSATION FAMILY?

The FDA product code for INTERA-SENSATION FAMILY is LNH.

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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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