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FDA 510(k)

PARA-PAK MACRO-CON

K-Number: K860034 · 1986-02-21

Decision Date1986-02-21
Product CodeLKS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PARA-PAK MACRO-CON is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1986-02-21 under 510(k) number K860034. The device is classified under product code LKS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 92 devices →

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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