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FDA 510(k)

PAO BIPOLAR COAGULATOR

K-Number: K840545 · 1984-02-08

ApplicantCimarron Instruments, Inc.
Decision Date1984-02-08
Product Code
DecisionUnknown

Device Summary

PAO BIPOLAR COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cimarron Instruments, Inc.. It received FDA 510(k) clearance on 1984-02-08 under 510(k) number K840545. FDA Decision: Unknown.

Frequently Asked Questions

What is the PAO BIPOLAR COAGULATOR?

PAO BIPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1984-02-08. The listed applicant is Cimarron Instruments, Inc.. The 510(k) number is K840545.

When did PAO BIPOLAR COAGULATOR receive FDA 510(k) clearance?

PAO BIPOLAR COAGULATOR received FDA 510(k) clearance on 1984-02-08, under 510(k) number K840545.

Who is the listed applicant for PAO BIPOLAR COAGULATOR?

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

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Other records listing Cimarron Instruments, Inc. as applicant

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.

K802972DUAL-TROLK801151DISPOSABLE SKIN RETRACTORK790293CIMARRON 1000 OR 1000-2

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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