FDA 510(k)

STERILE BLUNT FOR SINGLE USE

K-Number: K120420 · 2012-10-18

ApplicantShanghai Double Dove Industrial Co., Ltd.

Decision Date2012-10-18

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

STERILE BLUNT FOR SINGLE USE is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Double Dove Industrial Co., Ltd.. It received FDA 510(k) clearance on 2012-10-18 under 510(k) number K120420. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE BLUNT FOR SINGLE USE?

STERILE BLUNT FOR SINGLE USE is a medical device that received FDA 510(k) clearance on 2012-10-18. The listed applicant is Shanghai Double Dove Industrial Co., Ltd.. The 510(k) number is K120420.

When did STERILE BLUNT FOR SINGLE USE receive FDA 510(k) clearance?

STERILE BLUNT FOR SINGLE USE received FDA 510(k) clearance on 2012-10-18, under 510(k) number K120420.

Who is the listed applicant for STERILE BLUNT FOR SINGLE USE?

The FDA 510(k) record lists Shanghai Double Dove Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE BLUNT FOR SINGLE USE?

The FDA product code for STERILE BLUNT FOR SINGLE USE is FMI.

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Other records listing Shanghai Double Dove Industrial Co., Ltd. as applicant

K090929STERILE HYPODERMIC SYRINGE AND NEEDLE FOR SINGLE USE, STERILE INSULING SYRINGE FOR SINGLE USE WITH FIXED NEEDLE

Related Devices (Code: FMI)

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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.