STERILE PAN SET
K-Number: K842136 · 1984-07-06
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Device Summary
Frequently Asked Questions
What is the STERILE PAN SET?
STERILE PAN SET is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K842136.
When did STERILE PAN SET receive FDA 510(k) clearance?
STERILE PAN SET received FDA 510(k) clearance on 1984-07-06, under 510(k) number K842136.
Who is the listed applicant for STERILE PAN SET?
The FDA 510(k) record lists Medi-Plast Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE PAN SET?
The FDA product code for STERILE PAN SET is FRG.
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-Plast Intl., 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: FRG)
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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