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FDA 510(k)

EBI THERMAL THERAPY SYSTEM

K-Number: K963261 · 1996-09-27

ApplicantElectro-Biology, Inc.
Decision Date1996-09-27
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EBI THERMAL THERAPY 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 1996-09-27 under 510(k) number K963261. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBI THERMAL THERAPY SYSTEM?

EBI THERMAL THERAPY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-09-27. The listed applicant is Electro-Biology, Inc.. The 510(k) number is K963261.

When did EBI THERMAL THERAPY SYSTEM receive FDA 510(k) clearance?

EBI THERMAL THERAPY SYSTEM received FDA 510(k) clearance on 1996-09-27, under 510(k) number K963261.

Who is the listed applicant for EBI THERMAL THERAPY 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 THERMAL THERAPY SYSTEM?

The FDA product code for EBI THERMAL THERAPY SYSTEM is ILO.

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Other records listing Electro-Biology, Inc. 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.

K992333EBI OMEGA 21 SYSTEMK992367EBI XFIX DYNAFIX SYSTEM HA COATED SCREWSK991941EBI XFIX DFS RAIL SYSTEMK990303EBI OMEGA 21 SYSTEMK991092EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEMK990459EBI VUECATH ENDOSCOPIC SYSTEN

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Related Devices (Code: ILO)

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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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