FDA 510(k)

PARAGON MICRO-LOOPS

K-Number: K860022 · 1986-03-24

ApplicantParagon Medical and Scientific, Inc.

Decision Date1986-03-24

Product Code

DecisionSubstantially Equivalent

Device Summary

PARAGON MICRO-LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Medical and Scientific, Inc.. It received FDA 510(k) clearance on 1986-03-24 under 510(k) number K860022. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAGON MICRO-LOOPS?

PARAGON MICRO-LOOPS is a medical device that received FDA 510(k) clearance on 1986-03-24. The listed applicant is Paragon Medical and Scientific, Inc.. The 510(k) number is K860022.

When did PARAGON MICRO-LOOPS receive FDA 510(k) clearance?

PARAGON MICRO-LOOPS received FDA 510(k) clearance on 1986-03-24, under 510(k) number K860022.

Who is the listed applicant for PARAGON MICRO-LOOPS?

The FDA 510(k) record lists Paragon Medical and Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.