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FDA 510(k)

SYREX SYRINGE

K-Number: K913769 · 1992-01-23

ApplicantSpecial Machinery Co.
Decision Date1992-01-23
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYREX SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Special Machinery Co.. It received FDA 510(k) clearance on 1992-01-23 under 510(k) number K913769. 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 SYREX SYRINGE?

SYREX SYRINGE is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Special Machinery Co.. The 510(k) number is K913769.

When did SYREX SYRINGE receive FDA 510(k) clearance?

SYREX SYRINGE received FDA 510(k) clearance on 1992-01-23, under 510(k) number K913769.

Who is the listed applicant for SYREX SYRINGE?

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

What is the FDA product code for SYREX SYRINGE?

The FDA product code for SYREX 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.

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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