VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND
K-Number: K853179 · 1985-11-07
Advertisement
Device Summary
Frequently Asked Questions
What is the VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND?
VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND is a medical device that received FDA 510(k) clearance on 1985-11-07. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K853179.
When did VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND receive FDA 510(k) clearance?
VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND received FDA 510(k) clearance on 1985-11-07, under 510(k) number K853179.
Who is the listed applicant for VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND?
The FDA 510(k) record lists Keeler Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND?
The FDA product code for VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND is GZX.
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 Keeler Instruments, 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.
Related Devices (Code: GZX)
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