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FDA 510(k)

FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095

K-Number: K983338 · 1999-04-20

ApplicantNucletron Corp.
Decision Date1999-04-20
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 1999-04-20 under 510(k) number K983338. 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 FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095?

FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095 is a medical device that received FDA 510(k) clearance on 1999-04-20. The listed applicant is Nucletron Corp.. The 510(k) number is K983338.

When did FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095 receive FDA 510(k) clearance?

FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095 received FDA 510(k) clearance on 1999-04-20, under 510(k) number K983338.

Who is the listed applicant for FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095?

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 FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095?

The FDA product code for FREIBURG FLAP APPLICATOR SET, PART NUMBER 089.095 is JAQ.

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Other records listing Nucletron Corp. as applicant

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Related Devices (Code: 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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