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FDA 510(k)

DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE

K-Number: K103736 · 2011-06-10

ApplicantDmc Medical, Ltd.
Decision Date2011-06-10
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Dmc Medical, Ltd.. It received FDA 510(k) clearance on 2011-06-10 under 510(k) number K103736. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE?

DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE is a medical device that received FDA 510(k) clearance on 2011-06-10. The listed applicant is Dmc Medical, Ltd.. The 510(k) number is K103736.

When did DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE receive FDA 510(k) clearance?

DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE received FDA 510(k) clearance on 2011-06-10, under 510(k) number K103736.

Who is the listed applicant for DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE?

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

What is the FDA product code for DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE?

The FDA product code for DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE is FMF.

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Other records listing Dmc Medical, 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.

K992932CIPA (ADULTS) CIPI (INFANTS)K000704DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)

Related Devices (Code: FMF)

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.

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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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