HEAD & FOOT END DROP PEDI-CRIB
K-Number: K925817 · 1993-04-20
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Device Summary
Frequently Asked Questions
What is the HEAD & FOOT END DROP PEDI-CRIB?
HEAD & FOOT END DROP PEDI-CRIB is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Pedicraft, Inc.. The 510(k) number is K925817.
When did HEAD & FOOT END DROP PEDI-CRIB receive FDA 510(k) clearance?
HEAD & FOOT END DROP PEDI-CRIB received FDA 510(k) clearance on 1993-04-20, under 510(k) number K925817.
Who is the listed applicant for HEAD & FOOT END DROP PEDI-CRIB?
The FDA 510(k) record lists Pedicraft, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEAD & FOOT END DROP PEDI-CRIB?
The FDA product code for HEAD & FOOT END DROP PEDI-CRIB is FMS.
Other records listing Pedicraft, 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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