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FDA 510(k)

SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1

K-Number: K022959 · 2003-02-05

Decision Date2003-02-05
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1 is the device name listed in this FDA 510(k) record. The listed applicant is MDC Research , Ltd.. It received FDA 510(k) clearance on 2003-02-05 under 510(k) number K022959. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1?

SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1 is a medical device that received FDA 510(k) clearance on 2003-02-05. The listed applicant is MDC Research , Ltd.. The 510(k) number is K022959.

When did SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1 receive FDA 510(k) clearance?

SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1 received FDA 510(k) clearance on 2003-02-05, under 510(k) number K022959.

Who is the listed applicant for SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1?

The FDA 510(k) record lists MDC Research , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1?

The FDA product code for SAFESTEP SAFETY DENTAL CARTRIDGE INJECTOR, MODEL 33-00000-1 is EJI.

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.

Other records listing MDC Research , Ltd. 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.

Related Devices (Code: EJI)

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.

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.

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