RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS
K-Number: K891200 · 1989-04-06
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Device Summary
Frequently Asked Questions
What is the RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS?
RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS is a medical device that received FDA 510(k) clearance on 1989-04-06. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891200.
When did RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS receive FDA 510(k) clearance?
RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS received FDA 510(k) clearance on 1989-04-06, under 510(k) number K891200.
Who is the listed applicant for RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS?
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 RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS?
The FDA product code for RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS is LRW.
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: LRW)
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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