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FDA 510(k)

BUF-FIX

K-Number: K842728 · 1984-08-03

Decision Date1984-08-03
Product CodeIFP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

BUF-FIX is the device name listed in this FDA 510(k) record. The listed applicant is E K Ind., Inc.. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K842728. The device is classified under product code IFP. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

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.

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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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