WAYMOUTH'S MEDIUM MB 752/1
K-Number: K850224 · 1985-03-05
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Device Summary
Frequently Asked Questions
What is the WAYMOUTH'S MEDIUM MB 752/1?
WAYMOUTH'S MEDIUM MB 752/1 is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850224.
When did WAYMOUTH'S MEDIUM MB 752/1 receive FDA 510(k) clearance?
WAYMOUTH'S MEDIUM MB 752/1 received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850224.
Who is the listed applicant for WAYMOUTH'S MEDIUM MB 752/1?
The FDA 510(k) record lists Hazleton Research Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WAYMOUTH'S MEDIUM MB 752/1?
The FDA product code for WAYMOUTH'S MEDIUM MB 752/1 is KIT.
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 Hazleton Research 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: KIT)
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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