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FDA 510(k)

PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)

K-Number: K972749 · 1998-03-13

Decision Date1998-03-13
Product CodeHQR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) is the device name listed in this FDA 510(k) record. The listed applicant is C.M. Chance , Ltd.. It received FDA 510(k) clearance on 1998-03-13 under 510(k) number K972749. The device is classified under product code HQR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)?

PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) is a medical device that received FDA 510(k) clearance on 1998-03-13. The listed applicant is C.M. Chance , Ltd.. The 510(k) number is K972749.

When did PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) receive FDA 510(k) clearance?

PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) received FDA 510(k) clearance on 1998-03-13, under 510(k) number K972749.

Who is the listed applicant for PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)?

The FDA 510(k) record lists C.M. Chance , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S)?

The FDA product code for PAO BIPOLAR COAXIAL COAGULATOR (55-P15C/55-P18C/55-P18S/55-P19S/55-P20S) is HQR.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: HQR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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