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FDA 510(k)

HU-FRIEDY DENTAL CARTRIDGE SYRINGE

K-Number: K120659 · 2012-11-06

ApplicantHu-Friedy Mfg. Co., LLC
Decision Date2012-11-06
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HU-FRIEDY DENTAL CARTRIDGE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Hu-Friedy Mfg. Co., LLC. It received FDA 510(k) clearance on 2012-11-06 under 510(k) number K120659. 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 HU-FRIEDY DENTAL CARTRIDGE SYRINGE?

HU-FRIEDY DENTAL CARTRIDGE SYRINGE is a medical device that received FDA 510(k) clearance on 2012-11-06. The listed applicant is Hu-Friedy Mfg. Co., LLC. The 510(k) number is K120659.

When did HU-FRIEDY DENTAL CARTRIDGE SYRINGE receive FDA 510(k) clearance?

HU-FRIEDY DENTAL CARTRIDGE SYRINGE received FDA 510(k) clearance on 2012-11-06, under 510(k) number K120659.

Who is the listed applicant for HU-FRIEDY DENTAL CARTRIDGE SYRINGE?

The FDA 510(k) record lists Hu-Friedy Mfg. Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HU-FRIEDY DENTAL CARTRIDGE SYRINGE?

The FDA product code for HU-FRIEDY DENTAL CARTRIDGE SYRINGE is EJI.

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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.

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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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