B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG
K-Number: K942645 · 1994-07-27
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Device Summary
Frequently Asked Questions
What is the B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG?
B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG is a medical device that received FDA 510(k) clearance on 1994-07-27. The listed applicant is B & F Medical Products, Inc.. The 510(k) number is K942645.
When did B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG receive FDA 510(k) clearance?
B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG received FDA 510(k) clearance on 1994-07-27, under 510(k) number K942645.
Who is the listed applicant for B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG?
The FDA 510(k) record lists B & F Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG?
The FDA product code for B&F MEDICAL OXYGEN REG MECICAL OXY COMPRESS GAS REG is BXH.
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 B & F Medical Products, 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: BXH)
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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