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FDA 510(k)

MERRIES UNI-OSTEO, MODEL CS30250-CS10102

K-Number: K051698 · 2005-09-29

ApplicantMerries International, Inc.
Decision Date2005-09-29
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MERRIES UNI-OSTEO, MODEL CS30250-CS10102 is the device name listed in this FDA 510(k) record. The listed applicant is Merries International, Inc.. It received FDA 510(k) clearance on 2005-09-29 under 510(k) number K051698. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERRIES UNI-OSTEO, MODEL CS30250-CS10102?

MERRIES UNI-OSTEO, MODEL CS30250-CS10102 is a medical device that received FDA 510(k) clearance on 2005-09-29. The listed applicant is Merries International, Inc.. The 510(k) number is K051698.

When did MERRIES UNI-OSTEO, MODEL CS30250-CS10102 receive FDA 510(k) clearance?

MERRIES UNI-OSTEO, MODEL CS30250-CS10102 received FDA 510(k) clearance on 2005-09-29, under 510(k) number K051698.

Who is the listed applicant for MERRIES UNI-OSTEO, MODEL CS30250-CS10102?

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

What is the FDA product code for MERRIES UNI-OSTEO, MODEL CS30250-CS10102?

The FDA product code for MERRIES UNI-OSTEO, MODEL CS30250-CS10102 is MQV.

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Official Source

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