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FDA 510(k)

MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA-

K-Number: K850226 · 1985-03-07

ApplicantHazleton Research Products, Inc.
Decision Date1985-03-07
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA- 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 K850226. 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 MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA-?

MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA- 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 K850226.

When did MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA- receive FDA 510(k) clearance?

MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA- received FDA 510(k) clearance on 1985-03-07, under 510(k) number K850226.

Who is the listed applicant for MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA-?

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 MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA-?

The FDA product code for MCCOY'S MEDIUM 5A, IWAKATA & GRACE MODIFICA- is KIT.

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Other records listing Hazleton Research Products, Inc. as applicant

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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.

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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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