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FDA 510(k)

SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2

K-Number: K012266 · 2001-09-12

Decision Date2001-09-12
Product CodeMRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2 is the device name listed in this FDA 510(k) record. The listed applicant is National Custom Ent., Inc.. It received FDA 510(k) clearance on 2001-09-12 under 510(k) number K012266. The device is classified under product code MRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2?

SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2 is a medical device that received FDA 510(k) clearance on 2001-09-12. The listed applicant is National Custom Ent., Inc.. The 510(k) number is K012266.

When did SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2 receive FDA 510(k) clearance?

SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2 received FDA 510(k) clearance on 2001-09-12, under 510(k) number K012266.

Who is the listed applicant for SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2?

The FDA 510(k) record lists National Custom Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2?

The FDA product code for SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2 is MRZ.

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 National Custom Ent., Inc. 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 12 devices →

Related Devices (Code: MRZ)

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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