MEDPAR SURGICAL IMPLANTS
K-Number: K832283 · 1984-05-10
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Device Summary
Frequently Asked Questions
What is the MEDPAR SURGICAL IMPLANTS?
MEDPAR SURGICAL IMPLANTS is a medical device that received FDA 510(k) clearance on 1984-05-10. The listed applicant is Porex Medical. The 510(k) number is K832283.
When did MEDPAR SURGICAL IMPLANTS receive FDA 510(k) clearance?
MEDPAR SURGICAL IMPLANTS received FDA 510(k) clearance on 1984-05-10, under 510(k) number K832283.
Who is the listed applicant for MEDPAR SURGICAL IMPLANTS?
The FDA 510(k) record lists Porex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDPAR SURGICAL IMPLANTS?
The FDA product code for MEDPAR SURGICAL IMPLANTS is FWP.
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 Porex Medical 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: FWP)
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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