FDA 510(k)

SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE

K-Number: K941426 · 1994-06-22

Decision Date1994-06-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K941426. 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 SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE?

SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Symbiosis Corp.. The 510(k) number is K941426.

When did SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE receive FDA 510(k) clearance?

SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE received FDA 510(k) clearance on 1994-06-22, under 510(k) number K941426.

Who is the listed applicant for SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE?

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 REUSABLE MONOPOLAR ELECTROSURGICAL PROBE?

The FDA product code for SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE is GEI.

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Other records listing Symbiosis Corp. as applicant

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES K953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES K953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES K952432SYMBIOSIS BIPOLAR FORCEPS K951387SYMBIOSIS BIPOLAR SCISSORS K950286SYMBIOSIS BIPOLAR SCISSORS

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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.