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FDA 510(k)

KREATIV MODEL KV-1

K-Number: K940776 · 1994-12-21

ApplicantKreativ, Inc.
Decision Date1994-12-21
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KREATIV MODEL KV-1 is the device name listed in this FDA 510(k) record. The listed applicant is Kreativ, Inc.. It received FDA 510(k) clearance on 1994-12-21 under 510(k) number K940776. 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 KREATIV MODEL KV-1?

KREATIV MODEL KV-1 is a medical device that received FDA 510(k) clearance on 1994-12-21. The listed applicant is Kreativ, Inc.. The 510(k) number is K940776.

When did KREATIV MODEL KV-1 receive FDA 510(k) clearance?

KREATIV MODEL KV-1 received FDA 510(k) clearance on 1994-12-21, under 510(k) number K940776.

Who is the listed applicant for KREATIV MODEL KV-1?

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

What is the FDA product code for KREATIV MODEL KV-1?

The FDA product code for KREATIV MODEL KV-1 is KOJ.

Related Clinical Trials

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Other records listing Kreativ, 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.

K990060MACH 7K983227POWER BLOCKK980216KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6K962376KREATIV KURING LIGHT SYSTEM

Related Devices (Code: KOJ)

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.

K251425turbodent touchMectron S.P.A.K063236BETA-POWDERBrainbase CorporationK042872RONDOFLEX PLUS 360Kavo America CorporationK033675PROSMILE AIR POLISHER AND PROPHYLAXIS POWDERSirona Dental Systems GmbHK033215PREPAIRDanville Materials, Inc.K024105VELOPEX AQUACUT FLUID ABRASION UNITVelopex International, Inc.

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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