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FDA 510(k)

BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE

K-Number: K760722 · 1976-11-01

ApplicantBirtcher Corp.
Decision Date1976-11-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Birtcher Corp.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760722. 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 BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE?

BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Birtcher Corp.. The 510(k) number is K760722.

When did BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE receive FDA 510(k) clearance?

BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760722.

Who is the listed applicant for BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE?

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 BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE?

The FDA product code for BIRT-A-CHUCK DISPOSABLE ELECTR. HANDLE 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. 768K860718ELECTROSURGERY PENCIL, MODEL 767K854814SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33K854864BI-POLAR FORCEPSK850943MODEL 775 BIPOLAR COAGULATOR

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Related Devices (Code: GEI)

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.

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)Stryker InstrumentsK254196HARMONIC 1100 Shears (HAR1120); HARMONIC 1100 Shears (HAR1136)Ethicon Endo-Surgery, LLCK261070LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coatedCovidien, LLCK254185Potenza PrimeJeisys Medical IncorporatedK262364Ellian Enigma RF DeviceEllian CorpK253859Scarlet Pro (Scarlet Pro)VIOL Co., Ltd.

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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