Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT

K-Number: K860940 · 1986-05-02

Decision Date1986-05-02
Product CodeETF
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT is the device name listed in this FDA 510(k) record. The listed applicant is Micromedics, Inc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K860940. The device is classified under product code ETF. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT?

MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Micromedics, Inc.. The 510(k) number is K860940.

When did MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT receive FDA 510(k) clearance?

MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT received FDA 510(k) clearance on 1986-05-02, under 510(k) number K860940.

Who is the listed applicant for MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT?

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

What is the FDA product code for MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT?

The FDA product code for MICROMEDICS STERILE, DISPOSABLE ENT EXAM KIT is ETF.

Related Clinical Trials

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.

Other records listing Micromedics, 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.

View all 29 devices →

Related Devices (Code: ETF)

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.

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.

↑