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FDA 510(k)

POWER BLOCK

K-Number: K983227 · 1998-12-11

ApplicantKreativ, Inc.
Decision Date1998-12-11
Product CodeEIE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POWER BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Kreativ, Inc.. It received FDA 510(k) clearance on 1998-12-11 under 510(k) number K983227. The device is classified under product code EIE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER BLOCK?

POWER BLOCK is a medical device that received FDA 510(k) clearance on 1998-12-11. The listed applicant is Kreativ, Inc.. The 510(k) number is K983227.

When did POWER BLOCK receive FDA 510(k) clearance?

POWER BLOCK received FDA 510(k) clearance on 1998-12-11, under 510(k) number K983227.

Who is the listed applicant for POWER BLOCK?

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 POWER BLOCK?

The FDA product code for POWER BLOCK is EIE.

Related Clinical Trials

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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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 7K980216KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6K962376KREATIV KURING LIGHT SYSTEMK940776KREATIV MODEL KV-1

Related Devices (Code: EIE)

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.

K182118armor LCMavrik Dental Systems, Ltd.K151945Triumph Resin DamDenali CorporationK050318BARI-KAD PACKING DEVICEBioenvelop Agro, Inc.K043301GC TION GINGIVAL PROTECTORGC America, Inc.K040797BRITESMILE MASKING CREAMBritesmile, Inc.K022522PULPDENT PUTTY DAMPulpdent Corporation

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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