NEUTRAL BUFFERED FORMALIN 10%
K-Number: K830583 · 1983-03-17
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Device Summary
Frequently Asked Questions
What is the NEUTRAL BUFFERED FORMALIN 10%?
NEUTRAL BUFFERED FORMALIN 10% is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K830583.
When did NEUTRAL BUFFERED FORMALIN 10% receive FDA 510(k) clearance?
NEUTRAL BUFFERED FORMALIN 10% received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830583.
Who is the listed applicant for NEUTRAL BUFFERED FORMALIN 10%?
The FDA 510(k) record lists Surgipath Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEUTRAL BUFFERED FORMALIN 10%?
The FDA product code for NEUTRAL BUFFERED FORMALIN 10% is IFP.
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 Surgipath Medical Industries, 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: IFP)
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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