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FDA 510(k)

COLPO-MASTER

K-Number: K073053 · 2007-11-15

ApplicantUnited Products & Instruments, Inc.
Decision Date2007-11-15
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COLPO-MASTER is the device name listed in this FDA 510(k) record. The listed applicant is United Products & Instruments, Inc.. It received FDA 510(k) clearance on 2007-11-15 under 510(k) number K073053. The device is classified under product code HEX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLPO-MASTER?

COLPO-MASTER is a medical device that received FDA 510(k) clearance on 2007-11-15. The listed applicant is United Products & Instruments, Inc.. The 510(k) number is K073053.

When did COLPO-MASTER receive FDA 510(k) clearance?

COLPO-MASTER received FDA 510(k) clearance on 2007-11-15, under 510(k) number K073053.

Who is the listed applicant for COLPO-MASTER?

The FDA 510(k) record lists United Products & Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLPO-MASTER?

The FDA product code for COLPO-MASTER is HEX.

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Related Devices (Code: HEX)

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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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