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FDA 510(k)

NEUSTEIN LARYNGOSCOPE

K-Number: K901164 · 1990-10-09

ApplicantNeutech Corp.
Decision Date1990-10-09
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEUSTEIN LARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Neutech Corp.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K901164. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUSTEIN LARYNGOSCOPE?

NEUSTEIN LARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Neutech Corp.. The 510(k) number is K901164.

When did NEUSTEIN LARYNGOSCOPE receive FDA 510(k) clearance?

NEUSTEIN LARYNGOSCOPE received FDA 510(k) clearance on 1990-10-09, under 510(k) number K901164.

Who is the listed applicant for NEUSTEIN LARYNGOSCOPE?

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

What is the FDA product code for NEUSTEIN LARYNGOSCOPE?

The FDA product code for NEUSTEIN LARYNGOSCOPE is CCW.

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Related Devices (Code: CCW)

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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