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FDA 510(k)

DENTALOGIC

K-Number: K960270 · 1996-03-15

ApplicantProtecs Syringes International Corp.
Decision Date1996-03-15
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTALOGIC is the device name listed in this FDA 510(k) record. The listed applicant is Protecs Syringes International Corp.. It received FDA 510(k) clearance on 1996-03-15 under 510(k) number K960270. 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 DENTALOGIC?

DENTALOGIC is a medical device that received FDA 510(k) clearance on 1996-03-15. The listed applicant is Protecs Syringes International Corp.. The 510(k) number is K960270.

When did DENTALOGIC receive FDA 510(k) clearance?

DENTALOGIC received FDA 510(k) clearance on 1996-03-15, under 510(k) number K960270.

Who is the listed applicant for DENTALOGIC?

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

What is the FDA product code for DENTALOGIC?

The FDA product code for DENTALOGIC 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.

K171254LeEject 2 Dental Syringe and Needle SystemAdvanced Technology and Capital, Inc.K120659HU-FRIEDY DENTAL CARTRIDGE SYRINGEHu-Friedy Mfg. Co., LLCK113247ANESTHESIA INJECTION TOOL SETKi Works Co., Ltd.K082249MORPHEUSMeibach Tech LtdaK092943ASPIRATING SYRINGE, NON-ASPIRATING SYRINGEArnold Tuber IndustriesK083796MILTEX ASPIRATING SYRINGE, MILTEX PETITE ASPIRATING SYRINGE, MILTEX SELF-ASPIRATING SYRINGE, MILTEX LIGHTWEIGHTMiltex, Inc.

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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