FORMULATION HWS-64 EPA REG. NO. 47371-131
K-Number: K953011 · 1995-08-11
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Device Summary
Frequently Asked Questions
What is the FORMULATION HWS-64 EPA REG. NO. 47371-131?
FORMULATION HWS-64 EPA REG. NO. 47371-131 is a medical device that received FDA 510(k) clearance on 1995-08-11. The listed applicant is Huntington Laboratories, Inc.. The 510(k) number is K953011.
When did FORMULATION HWS-64 EPA REG. NO. 47371-131 receive FDA 510(k) clearance?
FORMULATION HWS-64 EPA REG. NO. 47371-131 received FDA 510(k) clearance on 1995-08-11, under 510(k) number K953011.
Who is the listed applicant for FORMULATION HWS-64 EPA REG. NO. 47371-131?
The FDA 510(k) record lists Huntington Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORMULATION HWS-64 EPA REG. NO. 47371-131?
The FDA product code for FORMULATION HWS-64 EPA REG. NO. 47371-131 is LRJ. This falls under the Clinical Lab category.
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 Huntington Laboratories, 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: LRJ)
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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