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FDA 510(k)

JETSTREAM CAVITY PREPARATION SYSTEM

K-Number: K955050 · 1996-03-07

ApplicantDove Systems, Inc.
Decision Date1996-03-07
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JETSTREAM CAVITY PREPARATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dove Systems, Inc.. It received FDA 510(k) clearance on 1996-03-07 under 510(k) number K955050. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JETSTREAM CAVITY PREPARATION SYSTEM?

JETSTREAM CAVITY PREPARATION SYSTEM is a medical device that received FDA 510(k) clearance on 1996-03-07. The listed applicant is Dove Systems, Inc.. The 510(k) number is K955050.

When did JETSTREAM CAVITY PREPARATION SYSTEM receive FDA 510(k) clearance?

JETSTREAM CAVITY PREPARATION SYSTEM received FDA 510(k) clearance on 1996-03-07, under 510(k) number K955050.

Who is the listed applicant for JETSTREAM CAVITY PREPARATION SYSTEM?

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

What is the FDA product code for JETSTREAM CAVITY PREPARATION SYSTEM?

The FDA product code for JETSTREAM CAVITY PREPARATION SYSTEM is KOJ.

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Related Devices (Code: KOJ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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