PARAFFIN INFILTRATION MEDIUM
K-Number: K831580 · 1983-06-17
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Device Summary
Frequently Asked Questions
What is the PARAFFIN INFILTRATION MEDIUM?
PARAFFIN INFILTRATION MEDIUM is a medical device that received FDA 510(k) clearance on 1983-06-17. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K831580.
When did PARAFFIN INFILTRATION MEDIUM receive FDA 510(k) clearance?
PARAFFIN INFILTRATION MEDIUM received FDA 510(k) clearance on 1983-06-17, under 510(k) number K831580.
Who is the listed applicant for PARAFFIN INFILTRATION MEDIUM?
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 PARAFFIN INFILTRATION MEDIUM?
The FDA product code for PARAFFIN INFILTRATION MEDIUM is KEO.
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: KEO)
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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