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FDA 510(k)

GREEN-LINE BIPOLAR COAGULATION UNIT

K-Number: K860479 · 1986-05-01

ApplicantGrieshaber & Co.
Decision Date1986-05-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GREEN-LINE BIPOLAR COAGULATION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1986-05-01 under 510(k) number K860479. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREEN-LINE BIPOLAR COAGULATION UNIT?

GREEN-LINE BIPOLAR COAGULATION UNIT is a medical device that received FDA 510(k) clearance on 1986-05-01. The listed applicant is Grieshaber & Co.. The 510(k) number is K860479.

When did GREEN-LINE BIPOLAR COAGULATION UNIT receive FDA 510(k) clearance?

GREEN-LINE BIPOLAR COAGULATION UNIT received FDA 510(k) clearance on 1986-05-01, under 510(k) number K860479.

Who is the listed applicant for GREEN-LINE BIPOLAR COAGULATION UNIT?

The FDA 510(k) record lists Grieshaber & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREEN-LINE BIPOLAR COAGULATION UNIT?

The FDA product code for GREEN-LINE BIPOLAR COAGULATION UNIT is GEI.

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Other records listing Grieshaber & Co. as applicant

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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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