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FDA 510(k)

NTH 101 UL

K-Number: K871177 · 1987-10-09

ApplicantAragona Medical, Inc.
Decision Date1987-10-09
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NTH 101 UL is the device name listed in this FDA 510(k) record. The listed applicant is Aragona Medical, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K871177. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NTH 101 UL?

NTH 101 UL is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Aragona Medical, Inc.. The 510(k) number is K871177.

When did NTH 101 UL receive FDA 510(k) clearance?

NTH 101 UL received FDA 510(k) clearance on 1987-10-09, under 510(k) number K871177.

Who is the listed applicant for NTH 101 UL?

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

What is the FDA product code for NTH 101 UL?

The FDA product code for NTH 101 UL is FMT.

Other records listing Aragona Medical, 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.

K871178MTC XI UL

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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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