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FDA 510(k)

JENSEN GOLD FOIL

K-Number: K022206 · 2002-08-29

ApplicantJensen Industries, Inc.
Decision Date2002-08-29
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JENSEN GOLD FOIL is the device name listed in this FDA 510(k) record. The listed applicant is Jensen Industries, Inc.. It received FDA 510(k) clearance on 2002-08-29 under 510(k) number K022206. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JENSEN GOLD FOIL?

JENSEN GOLD FOIL is a medical device that received FDA 510(k) clearance on 2002-08-29. The listed applicant is Jensen Industries, Inc.. The 510(k) number is K022206.

When did JENSEN GOLD FOIL receive FDA 510(k) clearance?

JENSEN GOLD FOIL received FDA 510(k) clearance on 2002-08-29, under 510(k) number K022206.

Who is the listed applicant for JENSEN GOLD FOIL?

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

What is the FDA product code for JENSEN GOLD FOIL?

The FDA product code for JENSEN GOLD FOIL is EJT.

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Other records listing Jensen Industries, 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.

K183408Jensen Shade Effect LiquidsK112806JENSEN ZIRCONIAK111743THE INSYNC CERAMIC SYSTEMK070114CREATION CP-ZI PORCELAINK050838THE LF-P CERAMIC SYSTEMK043201WILLI GELLER CREATION ZI PORCELAIN

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Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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