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FDA 510(k)

CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES

K-Number: K955772 · 1996-07-08

ApplicantTtk Biomed, Ltd.
Decision Date1996-07-08
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Ttk Biomed, Ltd.. It received FDA 510(k) clearance on 1996-07-08 under 510(k) number K955772. 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 CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES?

CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES is a medical device that received FDA 510(k) clearance on 1996-07-08. The listed applicant is Ttk Biomed, Ltd.. The 510(k) number is K955772.

When did CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES receive FDA 510(k) clearance?

CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES received FDA 510(k) clearance on 1996-07-08, under 510(k) number K955772.

Who is the listed applicant for CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES?

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

What is the FDA product code for CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES?

The FDA product code for CLINICARE STERILE DISPOSABLE SYRINGE/NEEDLES is FMI.

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Related Devices (Code: FMI)

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Official Source

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