PARA-PAK MACRO-CON
K-Number: K860034 · 1986-02-21
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Device Summary
Frequently Asked Questions
What is the PARA-PAK MACRO-CON?
PARA-PAK MACRO-CON is a medical device that received FDA 510(k) clearance on 1986-02-21. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K860034.
When did PARA-PAK MACRO-CON receive FDA 510(k) clearance?
PARA-PAK MACRO-CON received FDA 510(k) clearance on 1986-02-21, under 510(k) number K860034.
Who is the listed applicant for PARA-PAK MACRO-CON?
The FDA 510(k) record lists Meridian Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARA-PAK MACRO-CON?
The FDA product code for PARA-PAK MACRO-CON is LKS.
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 Meridian Diagnostics, 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: LKS)
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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