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FDA 510(k)

NEOLOOPS

K-Number: K810890 · 1981-08-31

ApplicantMedical Marketing Systems
Decision Date1981-08-31
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NEOLOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing Systems. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K810890. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOLOOPS?

NEOLOOPS is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is Medical Marketing Systems. The 510(k) number is K810890.

When did NEOLOOPS receive FDA 510(k) clearance?

NEOLOOPS received FDA 510(k) clearance on 1981-08-31, under 510(k) number K810890.

Who is the listed applicant for NEOLOOPS?

The FDA 510(k) record lists Medical Marketing Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEOLOOPS?

The FDA product code for NEOLOOPS is DWS.

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Related Devices (Code: DWS)

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.

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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.

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