MODEL 500 PEDIATRIC STRETCHER/CRIB
K-Number: K852422 · 1985-07-05
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Device Summary
Frequently Asked Questions
What is the MODEL 500 PEDIATRIC STRETCHER/CRIB?
MODEL 500 PEDIATRIC STRETCHER/CRIB is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Midmark Corp.. The 510(k) number is K852422.
When did MODEL 500 PEDIATRIC STRETCHER/CRIB receive FDA 510(k) clearance?
MODEL 500 PEDIATRIC STRETCHER/CRIB received FDA 510(k) clearance on 1985-07-05, under 510(k) number K852422.
Who is the listed applicant for MODEL 500 PEDIATRIC STRETCHER/CRIB?
The FDA 510(k) record lists Midmark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 500 PEDIATRIC STRETCHER/CRIB?
The FDA product code for MODEL 500 PEDIATRIC STRETCHER/CRIB 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 Midmark Corp. 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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