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FDA 510(k)

CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251

K-Number: K042304 · 2004-09-08

ApplicantSpectris Technologies, Inc.
Decision Date2004-09-08
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251 is the device name listed in this FDA 510(k) record. The listed applicant is Spectris Technologies, Inc.. It received FDA 510(k) clearance on 2004-09-08 under 510(k) number K042304. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251?

CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251 is a medical device that received FDA 510(k) clearance on 2004-09-08. The listed applicant is Spectris Technologies, Inc.. The 510(k) number is K042304.

When did CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251 receive FDA 510(k) clearance?

CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251 received FDA 510(k) clearance on 2004-09-08, under 510(k) number K042304.

Who is the listed applicant for CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251?

The FDA 510(k) record lists Spectris Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251?

The FDA product code for CHUNC JUNIOR MODEL# SM 242, CHUNC ADAPT MODEL# SM 251 is IOR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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