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FDA 510(k)

NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES

K-Number: K944355 · 1994-12-07

ApplicantNissho Corp.
Decision Date1994-12-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Nissho Corp.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K944355. 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 NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES?

NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Nissho Corp.. The 510(k) number is K944355.

When did NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES receive FDA 510(k) clearance?

NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES received FDA 510(k) clearance on 1994-12-07, under 510(k) number K944355.

Who is the listed applicant for NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES?

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

What is the FDA product code for NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES?

The FDA product code for NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES is FMF.

Related Clinical Trials

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.

Other records listing Nissho Corp. 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.

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.

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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