HEPES BUFFER IM IN NORMAL SALINE
K-Number: K844877 · 1985-02-25
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Device Summary
Frequently Asked Questions
What is the HEPES BUFFER IM IN NORMAL SALINE?
HEPES BUFFER IM IN NORMAL SALINE is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K844877.
When did HEPES BUFFER IM IN NORMAL SALINE receive FDA 510(k) clearance?
HEPES BUFFER IM IN NORMAL SALINE received FDA 510(k) clearance on 1985-02-25, under 510(k) number K844877.
Who is the listed applicant for HEPES BUFFER IM IN NORMAL SALINE?
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 HEPES BUFFER IM IN NORMAL SALINE?
The FDA product code for HEPES BUFFER IM IN NORMAL SALINE is KIP.
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: KIP)
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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