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FDA 510(k)

MODIFIED PARACON(TM) CONCENTRATION KIT

K-Number: K881649 · 1988-04-21

Decision Date1988-04-21
Product CodeLKS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFIED PARACON(TM) CONCENTRATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Para Scientific Co.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881649. 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 MODIFIED PARACON(TM) CONCENTRATION KIT?

MODIFIED PARACON(TM) CONCENTRATION KIT is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Para Scientific Co.. The 510(k) number is K881649.

When did MODIFIED PARACON(TM) CONCENTRATION KIT receive FDA 510(k) clearance?

MODIFIED PARACON(TM) CONCENTRATION KIT received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881649.

Who is the listed applicant for MODIFIED PARACON(TM) CONCENTRATION KIT?

The FDA 510(k) record lists Para Scientific Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED PARACON(TM) CONCENTRATION KIT?

The FDA product code for MODIFIED PARACON(TM) CONCENTRATION KIT 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 Para Scientific Co. 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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