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FDA 510(k)

NIPRO DISPOSABLE SYRINGES

K-Number: K030683 · 2003-10-31

Decision Date2003-10-31
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIPRO DISPOSABLE SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corp.. It received FDA 510(k) clearance on 2003-10-31 under 510(k) number K030683. 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 DISPOSABLE SYRINGES?

NIPRO DISPOSABLE SYRINGES is a medical device that received FDA 510(k) clearance on 2003-10-31. The listed applicant is Nipro Medical Corp.. The 510(k) number is K030683.

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

NIPRO DISPOSABLE SYRINGES received FDA 510(k) clearance on 2003-10-31, under 510(k) number K030683.

Who is the listed applicant for NIPRO DISPOSABLE SYRINGES?

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

What is the FDA product code for NIPRO DISPOSABLE SYRINGES?

The FDA product code for NIPRO DISPOSABLE SYRINGES 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 Nipro Medical 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.

View all 27 devices →

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

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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