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FDA 510(k)

MICROSELECTRON V3, MODEL 106.990

K-Number: K061354 · 2006-08-17

ApplicantNucletron Corporation
Decision Date2006-08-17
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICROSELECTRON V3, MODEL 106.990 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corporation. It received FDA 510(k) clearance on 2006-08-17 under 510(k) number K061354. 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 MICROSELECTRON V3, MODEL 106.990?

MICROSELECTRON V3, MODEL 106.990 is a medical device that received FDA 510(k) clearance on 2006-08-17. The listed applicant is Nucletron Corporation. The 510(k) number is K061354.

When did MICROSELECTRON V3, MODEL 106.990 receive FDA 510(k) clearance?

MICROSELECTRON V3, MODEL 106.990 received FDA 510(k) clearance on 2006-08-17, under 510(k) number K061354.

Who is the listed applicant for MICROSELECTRON V3, MODEL 106.990?

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

What is the FDA product code for MICROSELECTRON V3, MODEL 106.990?

The FDA product code for MICROSELECTRON V3, MODEL 106.990 is JAQ.

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Other records listing Nucletron Corporation 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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