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FDA 510(k)

ELECTROSURGICAL ENDOSCOPIC CORD

K-Number: K945717 · 1994-12-08

ApplicantBoston Surgical Products, Inc.
Decision Date1994-12-08
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL ENDOSCOPIC CORD is the device name listed in this FDA 510(k) record. The listed applicant is Boston Surgical Products, Inc.. It received FDA 510(k) clearance on 1994-12-08 under 510(k) number K945717. 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 ELECTROSURGICAL ENDOSCOPIC CORD?

ELECTROSURGICAL ENDOSCOPIC CORD is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Boston Surgical Products, Inc.. The 510(k) number is K945717.

When did ELECTROSURGICAL ENDOSCOPIC CORD receive FDA 510(k) clearance?

ELECTROSURGICAL ENDOSCOPIC CORD received FDA 510(k) clearance on 1994-12-08, under 510(k) number K945717.

Who is the listed applicant for ELECTROSURGICAL ENDOSCOPIC CORD?

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

What is the FDA product code for ELECTROSURGICAL ENDOSCOPIC CORD?

The FDA product code for ELECTROSURGICAL ENDOSCOPIC CORD is GEI.

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Other records listing Boston Surgical Products, Inc. as applicant

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K972311MODEL 20 BIPOLAR COAGULATORK972350MODEL 50 BIPOLAR COAGULATORK944947ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSK953012DISPOSABLE & REUSABLE SURGICAL CUTTING TOOLSK950375DISPOSABLE & REUSABLE BIPOLAR SUCTION COAGULATORK951912DISOPOSABLE & RESUABLE MONPOLAR CORD

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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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