LOW VOLUME INFUSTION SET
K-Number: K821624 · 1982-06-22
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Device Summary
Frequently Asked Questions
What is the LOW VOLUME INFUSTION SET?
LOW VOLUME INFUSTION SET is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Lifemed of California. The 510(k) number is K821624.
When did LOW VOLUME INFUSTION SET receive FDA 510(k) clearance?
LOW VOLUME INFUSTION SET received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821624.
Who is the listed applicant for LOW VOLUME INFUSTION SET?
The FDA 510(k) record lists Lifemed of California as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOW VOLUME INFUSTION SET?
The FDA product code for LOW VOLUME INFUSTION SET 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.
Other records listing Lifemed of California 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.
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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