ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES
K-Number: K925560 · 1994-08-30
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Device Summary
Frequently Asked Questions
What is the ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES?
ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-08-30. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K925560.
When did ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES receive FDA 510(k) clearance?
ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES received FDA 510(k) clearance on 1994-08-30, under 510(k) number K925560.
Who is the listed applicant for ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES?
The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES?
The FDA product code for ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES is HGI.
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 Zinnanti Surgical 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: HGI)
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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