OSI PAPOOSE BOARD
K-Number: K864879 · 1987-01-21
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Device Summary
Frequently Asked Questions
What is the OSI PAPOOSE BOARD?
OSI PAPOOSE BOARD is a medical device that received FDA 510(k) clearance on 1987-01-21. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K864879.
When did OSI PAPOOSE BOARD receive FDA 510(k) clearance?
OSI PAPOOSE BOARD received FDA 510(k) clearance on 1987-01-21, under 510(k) number K864879.
Who is the listed applicant for OSI PAPOOSE BOARD?
The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
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 Orthopedic Systems, 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.
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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