EBSS W/O CA & MG
K-Number: K850237 · 1985-03-07
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Device Summary
Frequently Asked Questions
What is the EBSS W/O CA & MG?
EBSS W/O CA & MG is a medical device that received FDA 510(k) clearance on 1985-03-07. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850237.
When did EBSS W/O CA & MG receive FDA 510(k) clearance?
EBSS W/O CA & MG received FDA 510(k) clearance on 1985-03-07, under 510(k) number K850237.
Who is the listed applicant for EBSS W/O CA & MG?
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 EBSS W/O CA & MG?
The FDA product code for EBSS W/O CA & MG is KIT.
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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