MEASURED VOLUME SOLUTION ADMINISTRATION SET
K-Number: K940054 · 1994-04-15
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Device Summary
Frequently Asked Questions
What is the MEASURED VOLUME SOLUTION ADMINISTRATION SET?
MEASURED VOLUME SOLUTION ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1994-04-15. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K940054.
When did MEASURED VOLUME SOLUTION ADMINISTRATION SET receive FDA 510(k) clearance?
MEASURED VOLUME SOLUTION ADMINISTRATION SET received FDA 510(k) clearance on 1994-04-15, under 510(k) number K940054.
Who is the listed applicant for MEASURED VOLUME SOLUTION ADMINISTRATION SET?
The FDA 510(k) record lists Puritas Health Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEASURED VOLUME SOLUTION ADMINISTRATION SET?
The FDA product code for MEASURED VOLUME SOLUTION ADMINISTRATION 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 Puritas Health Care, 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.
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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