STERILE CAST PADDING
K-Number: K801554 · 1980-08-04
Advertisement
Device Summary
Frequently Asked Questions
What is the STERILE CAST PADDING?
STERILE CAST PADDING is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Medi-Spec. The 510(k) number is K801554.
When did STERILE CAST PADDING receive FDA 510(k) clearance?
STERILE CAST PADDING received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801554.
Who is the listed applicant for STERILE CAST PADDING?
The FDA 510(k) record lists Medi-Spec as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE CAST PADDING?
The FDA product code for STERILE CAST PADDING is HIX.
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 Medi-Spec 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: HIX)
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.
Advertisement