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FDA 510(k)

JETLITE

K-Number: K963110 · 1996-10-24

ApplicantJ. Morita USA, Inc.
Decision Date1996-10-24
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JETLITE is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 1996-10-24 under 510(k) number K963110. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JETLITE?

JETLITE is a medical device that received FDA 510(k) clearance on 1996-10-24. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K963110.

When did JETLITE receive FDA 510(k) clearance?

JETLITE received FDA 510(k) clearance on 1996-10-24, under 510(k) number K963110.

Who is the listed applicant for JETLITE?

The FDA 510(k) record lists J. Morita USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JETLITE?

The FDA product code for JETLITE is EBZ.

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Other records listing J. Morita USA, Inc. as applicant

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Related Devices (Code: EBZ)

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.

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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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