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FDA 510(k)

EBI VUECATH ENDOSCOPIC SPINAL SYSTEM

K-Number: K982484 · 1998-10-08

ApplicantElectro-Biology, Inc.
Decision Date1998-10-08
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EBI VUECATH ENDOSCOPIC SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Biology, Inc.. It received FDA 510(k) clearance on 1998-10-08 under 510(k) number K982484. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBI VUECATH ENDOSCOPIC SPINAL SYSTEM?

EBI VUECATH ENDOSCOPIC SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-08. The listed applicant is Electro-Biology, Inc.. The 510(k) number is K982484.

When did EBI VUECATH ENDOSCOPIC SPINAL SYSTEM receive FDA 510(k) clearance?

EBI VUECATH ENDOSCOPIC SPINAL SYSTEM received FDA 510(k) clearance on 1998-10-08, under 510(k) number K982484.

Who is the listed applicant for EBI VUECATH ENDOSCOPIC SPINAL SYSTEM?

The FDA 510(k) record lists Electro-Biology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EBI VUECATH ENDOSCOPIC SPINAL SYSTEM?

The FDA product code for EBI VUECATH ENDOSCOPIC SPINAL SYSTEM is HRX.

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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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