CRADLING SYSTEM
K-Number: K761032 · 1977-01-26
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Device Summary
Frequently Asked Questions
What is the CRADLING SYSTEM?
CRADLING SYSTEM is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Medin Corp.. The 510(k) number is K761032.
When did CRADLING SYSTEM receive FDA 510(k) clearance?
CRADLING SYSTEM received FDA 510(k) clearance on 1977-01-26, under 510(k) number K761032.
Who is the listed applicant for CRADLING SYSTEM?
The FDA 510(k) record lists Medin Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRADLING SYSTEM?
The FDA product code for CRADLING SYSTEM is FLE.
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 Medin 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: FLE)
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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