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FDA 510(k)

MIDDLE EAR VIEWER AND FLUID COLLECTOR

K-Number: K862903 · 1986-11-24

ApplicantSteven K. Juhn
Decision Date1986-11-24
Product CodeJZF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MIDDLE EAR VIEWER AND FLUID COLLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Steven K. Juhn. It received FDA 510(k) clearance on 1986-11-24 under 510(k) number K862903. The device is classified under product code JZF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDDLE EAR VIEWER AND FLUID COLLECTOR?

MIDDLE EAR VIEWER AND FLUID COLLECTOR is a medical device that received FDA 510(k) clearance on 1986-11-24. The listed applicant is Steven K. Juhn. The 510(k) number is K862903.

When did MIDDLE EAR VIEWER AND FLUID COLLECTOR receive FDA 510(k) clearance?

MIDDLE EAR VIEWER AND FLUID COLLECTOR received FDA 510(k) clearance on 1986-11-24, under 510(k) number K862903.

Who is the listed applicant for MIDDLE EAR VIEWER AND FLUID COLLECTOR?

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

What is the FDA product code for MIDDLE EAR VIEWER AND FLUID COLLECTOR?

The FDA product code for MIDDLE EAR VIEWER AND FLUID COLLECTOR is JZF.

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Related Devices (Code: JZF)

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.

K973587EXMOOR TYMPANOCENTESIS KIT (TK/1)Exmoor Plastics , Ltd.K853589SHAH SELF-CLEARING MASTOID SUCTION TUBEDowns Surgical , Ltd.K841357MICRO FLUID APPLICATORTreace Medical, Inc.K822010RIGID SUCTION TIPS & RELATED ITEMSKelleher Corp.

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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