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FDA 510(k)

JP CAST 40

K-Number: K011331 · 2001-06-22

ApplicantJeneric/Pentron, Inc.
Decision Date2001-06-22
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JP CAST 40 is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric/Pentron, Inc.. It received FDA 510(k) clearance on 2001-06-22 under 510(k) number K011331. 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 JP CAST 40?

JP CAST 40 is a medical device that received FDA 510(k) clearance on 2001-06-22. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K011331.

When did JP CAST 40 receive FDA 510(k) clearance?

JP CAST 40 received FDA 510(k) clearance on 2001-06-22, under 510(k) number K011331.

Who is the listed applicant for JP CAST 40?

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

What is the FDA product code for JP CAST 40?

The FDA product code for JP CAST 40 is EJT.

Other records listing Jeneric/Pentron, 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.

K020499BOND-3 ADHESIVEK013543BOND-1 C & BK013542DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)K012231AVANTE MICRO CRYSTAL SYSTEMK011748FIRST FILL R.C.S.K010957QUELL DESENSITIZER

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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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