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FDA 510(k)

INTERA FAMILY

K-Number: K030520 · 2003-03-06

ApplicantPhilips Medical Systems North America Co.
Decision Date2003-03-06
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERA FAMILY 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 2003-03-06 under 510(k) number K030520. 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 FAMILY?

INTERA FAMILY is a medical device that received FDA 510(k) clearance on 2003-03-06. The listed applicant is Philips Medical Systems North America Co.. The 510(k) number is K030520.

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

INTERA FAMILY received FDA 510(k) clearance on 2003-03-06, under 510(k) number K030520.

Who is the listed applicant for INTERA FAMILY?

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 INTERA FAMILY?

The FDA product code for INTERA 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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