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FDA 510(k)

SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B

K-Number: K984561 · 1999-02-04

ApplicantMsr, Inc.
Decision Date1999-02-04
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B is the device name listed in this FDA 510(k) record. The listed applicant is Msr, Inc.. It received FDA 510(k) clearance on 1999-02-04 under 510(k) number K984561. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B?

SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B is a medical device that received FDA 510(k) clearance on 1999-02-04. The listed applicant is Msr, Inc.. The 510(k) number is K984561.

When did SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B receive FDA 510(k) clearance?

SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B received FDA 510(k) clearance on 1999-02-04, under 510(k) number K984561.

Who is the listed applicant for SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B?

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

What is the FDA product code for SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B?

The FDA product code for SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B is FPA.

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.

Related Devices (Code: FPA)

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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