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FDA 510(k)

ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES

K-Number: K900176 · 1990-04-10

ApplicantMachida, Inc.
Decision Date1990-04-10
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Machida, Inc.. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K900176. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES?

ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Machida, Inc.. The 510(k) number is K900176.

When did ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES receive FDA 510(k) clearance?

ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES received FDA 510(k) clearance on 1990-04-10, under 510(k) number K900176.

Who is the listed applicant for ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES?

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

What is the FDA product code for ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES?

The FDA product code for ENT-2 FLEXIBLE NASOPHARYGNO-LARYNGOSCOPES is EOB.

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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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