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FDA 510(k)

SYMBIOSIS BIPOLAR SCISSORS

K-Number: K950286 · 1995-02-03

ApplicantSymbiosis Corp.
Decision Date1995-02-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS BIPOLAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1995-02-03 under 510(k) number K950286. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMBIOSIS BIPOLAR SCISSORS?

SYMBIOSIS BIPOLAR SCISSORS is a medical device that received FDA 510(k) clearance on 1995-02-03. The listed applicant is Symbiosis Corp.. The 510(k) number is K950286.

When did SYMBIOSIS BIPOLAR SCISSORS receive FDA 510(k) clearance?

SYMBIOSIS BIPOLAR SCISSORS received FDA 510(k) clearance on 1995-02-03, under 510(k) number K950286.

Who is the listed applicant for SYMBIOSIS BIPOLAR SCISSORS?

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

What is the FDA product code for SYMBIOSIS BIPOLAR SCISSORS?

The FDA product code for SYMBIOSIS BIPOLAR SCISSORS is GCJ.

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Other records listing Symbiosis 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK946238SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS

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Related Devices (Code: GCJ)

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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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