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FDA 510(k)

ELECTROSURGERY PENCIL, MODEL 767

K-Number: K860718 · 1986-03-24

ApplicantBirtcher Corp.
Decision Date1986-03-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGERY PENCIL, MODEL 767 is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1986-03-24 under 510(k) number K860718. 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 ELECTROSURGERY PENCIL, MODEL 767?

ELECTROSURGERY PENCIL, MODEL 767 is a medical device that received FDA 510(k) clearance on 1986-03-24. The listed applicant is Birtcher Corp.. The 510(k) number is K860718.

When did ELECTROSURGERY PENCIL, MODEL 767 receive FDA 510(k) clearance?

ELECTROSURGERY PENCIL, MODEL 767 received FDA 510(k) clearance on 1986-03-24, under 510(k) number K860718.

Who is the listed applicant for ELECTROSURGERY PENCIL, MODEL 767?

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

What is the FDA product code for ELECTROSURGERY PENCIL, MODEL 767?

The FDA product code for ELECTROSURGERY PENCIL, MODEL 767 is GEI.

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Other records listing Birtcher Corp. 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.

K881328MODEL 375 ECGK860687BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768K854814SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33K854864BI-POLAR FORCEPSK850943MODEL 775 BIPOLAR COAGULATORK850668ELECTROSURGICAL UNIT 774

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Related Devices (Code: GEI)

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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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