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FDA 510(k)

HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE

K-Number: K030572 · 2003-04-01

ApplicantHenke Sass Wolf of America, Inc.
Decision Date2003-04-01
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Henke Sass Wolf of America, Inc.. It received FDA 510(k) clearance on 2003-04-01 under 510(k) number K030572. 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 HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE?

HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE is a medical device that received FDA 510(k) clearance on 2003-04-01. The listed applicant is Henke Sass Wolf of America, Inc.. The 510(k) number is K030572.

When did HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE receive FDA 510(k) clearance?

HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE received FDA 510(k) clearance on 2003-04-01, under 510(k) number K030572.

Who is the listed applicant for HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE?

The FDA 510(k) record lists Henke Sass Wolf of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE?

The FDA product code for HENKE SASS WOLF OF AMERICA NASOPHARYNGOSCOPE is EOB.

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Other records listing Henke Sass Wolf of America, 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.

K080560HENKE SASS WOLF OF AMERICA ARTHROSCOPEK050163HENKE SASS WOLF OF AMERICA BARIATRIC LAPAROSCOPEK013611HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPEK991563CONTINUOUS FLOW HYSTERO-RESECTOSCOPE, KNIFE ELECTRODE, SPIKE ELECTRODE, VAPORISATION ELECTRODE, COAGULATION ELECTRODE, CK983067FINE-JECTK981751SINUSCOPE AND ACCESSORIES

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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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