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FDA 510(k)

MONOJECT PLASTIC DENTAL INJ. SYRINGE

K-Number: K792541 · 1980-02-01

ApplicantSherwood Medical Co.
Decision Date1980-02-01
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MONOJECT PLASTIC DENTAL INJ. SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1980-02-01 under 510(k) number K792541. 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 MONOJECT PLASTIC DENTAL INJ. SYRINGE?

MONOJECT PLASTIC DENTAL INJ. SYRINGE is a medical device that received FDA 510(k) clearance on 1980-02-01. The listed applicant is Sherwood Medical Co.. The 510(k) number is K792541.

When did MONOJECT PLASTIC DENTAL INJ. SYRINGE receive FDA 510(k) clearance?

MONOJECT PLASTIC DENTAL INJ. SYRINGE received FDA 510(k) clearance on 1980-02-01, under 510(k) number K792541.

Who is the listed applicant for MONOJECT PLASTIC DENTAL INJ. SYRINGE?

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

What is the FDA product code for MONOJECT PLASTIC DENTAL INJ. SYRINGE?

The FDA product code for MONOJECT PLASTIC DENTAL INJ. SYRINGE is EJI.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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