BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO
K-Number: K930060 · 1993-11-12
Advertisement
Device Summary
Frequently Asked Questions
What is the BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO?
BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Buffalo Filter Co., Inc.. The 510(k) number is K930060.
When did BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO receive FDA 510(k) clearance?
BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO received FDA 510(k) clearance on 1993-11-12, under 510(k) number K930060.
Who is the listed applicant for BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO?
The FDA 510(k) record lists Buffalo Filter Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO?
The FDA product code for BUFF. FILTER REPLACEMENT FILTER #BST312CO,BST306CO is FYD.
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 Buffalo Filter Co., 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: FYD)
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