VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED
K-Number: K853180 · 1985-10-28
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Device Summary
Frequently Asked Questions
What is the VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED?
VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED is a medical device that received FDA 510(k) clearance on 1985-10-28. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K853180.
When did VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED receive FDA 510(k) clearance?
VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED received FDA 510(k) clearance on 1985-10-28, under 510(k) number K853180.
Who is the listed applicant for VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED?
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 MICROS INSTR-LONG R OR L HANDED?
The FDA product code for VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED 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.
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