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FDA 510(k)

ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068

K-Number: K983337 · 1999-04-02

ApplicantNucletron Corp.
Decision Date1999-04-02
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 1999-04-02 under 510(k) number K983337. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068?

ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 is a medical device that received FDA 510(k) clearance on 1999-04-02. The listed applicant is Nucletron Corp.. The 510(k) number is K983337.

When did ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 receive FDA 510(k) clearance?

ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 received FDA 510(k) clearance on 1999-04-02, under 510(k) number K983337.

Who is the listed applicant for ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068?

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

What is the FDA product code for ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068?

The FDA product code for ROTTERDAM NASOPHAYRNX MOULD SET, PART #089.068 is JAQ.

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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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