FDA 510(k)

BOND-ON 4

K-Number: K951783 · 1995-06-02

Decision Date1995-06-02

Product CodeEJT

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

BOND-ON 4 is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Corp.. It received FDA 510(k) clearance on 1995-06-02 under 510(k) number K951783. 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 BOND-ON 4?

BOND-ON 4 is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is Degussa Corp.. The 510(k) number is K951783.

When did BOND-ON 4 receive FDA 510(k) clearance?

BOND-ON 4 received FDA 510(k) clearance on 1995-06-02, under 510(k) number K951783.

Who is the listed applicant for BOND-ON 4?

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

What is the FDA product code for BOND-ON 4?

The FDA product code for BOND-ON 4 is EJT.

Other records listing Degussa Corp. 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.

K973288STABILOR HN K972910PORS ON LITE K960256DEGUDENT LS K960226DG 88 K960104BIOCCLUS 4 K955465DEGUPRINT

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Related Devices (Code: EJT)

K052463PROMETAL HN86Prometal Technologies K041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KG K040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KG K040043NDX-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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.