FDA 510(k)

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES

K-Number: K953453 · 1996-01-17

Decision Date1996-01-17

Product CodeFAS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1996-01-17 under 510(k) number K953453. The device is classified under product code FAS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES?

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES is a medical device that received FDA 510(k) clearance on 1996-01-17. The listed applicant is Symbiosis Corp.. The 510(k) number is K953453.

When did SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES receive FDA 510(k) clearance?

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES received FDA 510(k) clearance on 1996-01-17, under 510(k) number K953453.

Who is the listed applicant for SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES?

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 MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES?

The FDA product code for SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES is FAS.

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Other records listing Symbiosis Corp. as applicant

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES K953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES K952432SYMBIOSIS BIPOLAR FORCEPS K951387SYMBIOSIS BIPOLAR SCISSORS K950286SYMBIOSIS BIPOLAR SCISSORS K946238SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS

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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.