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FDA 510(k)

SYMBIOSIS HEMOSTATIC WAND

K-Number: K925410 · 1993-02-23

ApplicantSymbiosis Corp.
Decision Date1993-02-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS HEMOSTATIC WAND is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1993-02-23 under 510(k) number K925410. 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 HEMOSTATIC WAND?

SYMBIOSIS HEMOSTATIC WAND is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is Symbiosis Corp.. The 510(k) number is K925410.

When did SYMBIOSIS HEMOSTATIC WAND receive FDA 510(k) clearance?

SYMBIOSIS HEMOSTATIC WAND received FDA 510(k) clearance on 1993-02-23, under 510(k) number K925410.

Who is the listed applicant for SYMBIOSIS HEMOSTATIC WAND?

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 HEMOSTATIC WAND?

The FDA product code for SYMBIOSIS HEMOSTATIC WAND 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 SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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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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