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FDA 510(k)

FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE

K-Number: K895245 · 1989-11-17

ApplicantOptimed Technologies, Inc.
Decision Date1989-11-17
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Optimed Technologies, Inc.. It received FDA 510(k) clearance on 1989-11-17 under 510(k) number K895245. 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 FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE?

FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 1989-11-17. The listed applicant is Optimed Technologies, Inc.. The 510(k) number is K895245.

When did FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE receive FDA 510(k) clearance?

FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE received FDA 510(k) clearance on 1989-11-17, under 510(k) number K895245.

Who is the listed applicant for FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE?

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

What is the FDA product code for FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE?

The FDA product code for FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE is EOB.

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Other records listing Optimed Technologies, Inc. as applicant

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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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