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FDA 510(k)

SYMBIOSIS BIPOLAR FORCEPS

K-Number: K952432 · 1995-07-05

ApplicantSymbiosis Corp.
Decision Date1995-07-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1995-07-05 under 510(k) number K952432. 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 BIPOLAR FORCEPS?

SYMBIOSIS BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1995-07-05. The listed applicant is Symbiosis Corp.. The 510(k) number is K952432.

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

SYMBIOSIS BIPOLAR FORCEPS received FDA 510(k) clearance on 1995-07-05, under 510(k) number K952432.

Who is the listed applicant for SYMBIOSIS BIPOLAR FORCEPS?

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 FORCEPS?

The FDA product code for SYMBIOSIS BIPOLAR FORCEPS is GEI.

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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 ELECTRODESK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORSK946238SYMBIOSIS 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.

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