SUBCUTANEOUS INFUSION SETS, MSR MODEL A & B
K-Number: K984561 · 1999-02-04
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Device Summary
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
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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