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FDA 510(k)

R & D DESIGNATION AP-035

K-Number: K010414 · 2001-03-27

ApplicantJensen Industries, Inc.
Decision Date2001-03-27
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

R & D DESIGNATION AP-035 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 2001-03-27 under 510(k) number K010414. 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 R & D DESIGNATION AP-035?

R & D DESIGNATION AP-035 is a medical device that received FDA 510(k) clearance on 2001-03-27. The listed applicant is Jensen Industries, Inc.. The 510(k) number is K010414.

When did R & D DESIGNATION AP-035 receive FDA 510(k) clearance?

R & D DESIGNATION AP-035 received FDA 510(k) clearance on 2001-03-27, under 510(k) number K010414.

Who is the listed applicant for R & D DESIGNATION AP-035?

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 R & D DESIGNATION AP-035?

The FDA product code for R & D DESIGNATION AP-035 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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