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)

WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE

K-Number: K914181 · 1991-12-10

Decision Date1991-12-10
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1991-12-10 under 510(k) number K914181. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE?

WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1991-12-10. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K914181.

When did WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE receive FDA 510(k) clearance?

WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE received FDA 510(k) clearance on 1991-12-10, under 510(k) number K914181.

Who is the listed applicant for WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE?

The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE?

The FDA product code for WANG/MILL-ROSE TRANSBRONCHIAL ASPIRATION NEEDLE is EOQ.

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 Mill-Rose Laboratory 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 46 devices →

Related Devices (Code: EOQ)

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.

↑