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FDA 510(k)

ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE

K-Number: K092943 · 2009-12-11

ApplicantArnold Tuber Industries
Decision Date2009-12-11
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Arnold Tuber Industries. It received FDA 510(k) clearance on 2009-12-11 under 510(k) number K092943. 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 ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE?

ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE is a medical device that received FDA 510(k) clearance on 2009-12-11. The listed applicant is Arnold Tuber Industries. The 510(k) number is K092943.

When did ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE receive FDA 510(k) clearance?

ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE received FDA 510(k) clearance on 2009-12-11, under 510(k) number K092943.

Who is the listed applicant for ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE?

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

What is the FDA product code for ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE?

The FDA product code for ASPIRATING SYRINGE, NON-ASPIRATING 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 LtdaK083796MILTEX ASPIRATING SYRINGE, MILTEX PETITE ASPIRATING SYRINGE, MILTEX SELF-ASPIRATING SYRINGE, MILTEX LIGHTWEIGHTMiltex, Inc.K081694DENJECTORDxm Co., Ltd.

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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