RIVER VIAL ADAPTER
K-Number: K933335 · 1994-03-01
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Device Summary
Frequently Asked Questions
What is the RIVER VIAL ADAPTER?
RIVER VIAL ADAPTER is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is River Medical, Inc.. The 510(k) number is K933335.
When did RIVER VIAL ADAPTER receive FDA 510(k) clearance?
RIVER VIAL ADAPTER received FDA 510(k) clearance on 1994-03-01, under 510(k) number K933335.
Who is the listed applicant for RIVER VIAL ADAPTER?
The FDA 510(k) record lists River Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIVER VIAL ADAPTER?
The FDA product code for RIVER VIAL ADAPTER is FMF.
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 River Medical, 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: FMF)
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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