MERIVAARA CRIB TROLLEY-MODEL 381
K-Number: K852173 · 1985-06-17
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Device Summary
Frequently Asked Questions
What is the MERIVAARA CRIB TROLLEY-MODEL 381?
MERIVAARA CRIB TROLLEY-MODEL 381 is a medical device that received FDA 510(k) clearance on 1985-06-17. The listed applicant is Daun International, Inc.. The 510(k) number is K852173.
When did MERIVAARA CRIB TROLLEY-MODEL 381 receive FDA 510(k) clearance?
MERIVAARA CRIB TROLLEY-MODEL 381 received FDA 510(k) clearance on 1985-06-17, under 510(k) number K852173.
Who is the listed applicant for MERIVAARA CRIB TROLLEY-MODEL 381?
The FDA 510(k) record lists Daun International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERIVAARA CRIB TROLLEY-MODEL 381?
The FDA product code for MERIVAARA CRIB TROLLEY-MODEL 381 is FMS.
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 Daun International, 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: FMS)
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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