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FDA 510(k)

NERVE BLOCK INFUSION KIT

K-Number: K984502 · 1999-03-04

ApplicantI-Flow Corp.
Decision Date1999-03-04
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NERVE BLOCK INFUSION KIT is the device name listed in this FDA 510(k) record. The listed applicant is I-Flow Corp.. It received FDA 510(k) clearance on 1999-03-04 under 510(k) number K984502. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NERVE BLOCK INFUSION KIT?

NERVE BLOCK INFUSION KIT is a medical device that received FDA 510(k) clearance on 1999-03-04. The listed applicant is I-Flow Corp.. The 510(k) number is K984502.

When did NERVE BLOCK INFUSION KIT receive FDA 510(k) clearance?

NERVE BLOCK INFUSION KIT received FDA 510(k) clearance on 1999-03-04, under 510(k) number K984502.

Who is the listed applicant for NERVE BLOCK INFUSION KIT?

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

What is the FDA product code for NERVE BLOCK INFUSION KIT?

The FDA product code for NERVE BLOCK INFUSION KIT is MEB.

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 I-Flow 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 41 devices →

Related Devices (Code: MEB)

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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