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FDA 510(k)

PAROJECT ANESTHETIC SYRINGE

K-Number: K904279 · 1990-12-07

ApplicantRonvig Instruments, Ltd.
Decision Date1990-12-07
Product CodeEGM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PAROJECT ANESTHETIC SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Ronvig Instruments, Ltd.. It received FDA 510(k) clearance on 1990-12-07 under 510(k) number K904279. The device is classified under product code EGM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAROJECT ANESTHETIC SYRINGE?

PAROJECT ANESTHETIC SYRINGE is a medical device that received FDA 510(k) clearance on 1990-12-07. The listed applicant is Ronvig Instruments, Ltd.. The 510(k) number is K904279.

When did PAROJECT ANESTHETIC SYRINGE receive FDA 510(k) clearance?

PAROJECT ANESTHETIC SYRINGE received FDA 510(k) clearance on 1990-12-07, under 510(k) number K904279.

Who is the listed applicant for PAROJECT ANESTHETIC SYRINGE?

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

What is the FDA product code for PAROJECT ANESTHETIC SYRINGE?

The FDA product code for PAROJECT ANESTHETIC SYRINGE is EGM.

Related Clinical Trials

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Other records listing Ronvig Instruments, 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.

K002168ASPIJECT SELF-ASPIRATING DENTAL INJECTION SYRINGE

Related Devices (Code: EGM)

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.

K243427QuickSleeper 5DentalhitecK083811W&H HANDPIECE ANESTO, MODEL: RA-5W&H Dentalwerk Buermoos GmbHK964802CYBERJET LOCAL ANESTHESIA SYSTEMIntra Vantage, Inc.K962017HYPODERMIC JET INJECTION APPARATUSAmerican Jet Injector Corp.K864294HENKE-JECT PRESSURE SYRINGE (MODIFICATION)Smith & Nephew, Inc.K864732GRADTECH SYRINGE SYSTEMGradtech

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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