BUF-FIX
K-Number: K842728 · 1984-08-03
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Device Summary
Frequently Asked Questions
What is the BUF-FIX?
BUF-FIX is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is E K Ind., Inc.. The 510(k) number is K842728.
When did BUF-FIX receive FDA 510(k) clearance?
BUF-FIX received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842728.
Who is the listed applicant for BUF-FIX?
The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUF-FIX?
The FDA product code for BUF-FIX is IFP.
Other records listing E K Ind., 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: IFP)
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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