GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN
K-Number: K864193 · 1986-11-17
Advertisement
Device Summary
Frequently Asked Questions
What is the GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN?
GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN is a medical device that received FDA 510(k) clearance on 1986-11-17. The listed applicant is Gaw, Inc.. The 510(k) number is K864193.
When did GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN receive FDA 510(k) clearance?
GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN received FDA 510(k) clearance on 1986-11-17, under 510(k) number K864193.
Who is the listed applicant for GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN?
The FDA 510(k) record lists Gaw, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN?
The FDA product code for GILBAUGH ASPIRATING BIOPSY SYRINGE/NEEDLE/GUN is GDM.
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.
Related Devices (Code: GDM)
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.
Advertisement