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FDA 510(k)

EBSS W/O CA & MG

K-Number: K850237 · 1985-03-07

Decision Date1985-03-07
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

EBSS W/O CA & MG is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Research Products, Inc.. It received FDA 510(k) clearance on 1985-03-07 under 510(k) number K850237. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 47 devices →

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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