NON-INSULATED SCISSORS
K-Number: K935073 · 1994-01-31
Advertisement
Device Summary
Frequently Asked Questions
What is the NON-INSULATED SCISSORS?
NON-INSULATED SCISSORS is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K935073.
When did NON-INSULATED SCISSORS receive FDA 510(k) clearance?
NON-INSULATED SCISSORS received FDA 510(k) clearance on 1994-01-31, under 510(k) number K935073.
Who is the listed applicant for NON-INSULATED SCISSORS?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-INSULATED SCISSORS?
The FDA product code for NON-INSULATED SCISSORS is GCJ.
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 KARL STORZ Endoscopy-America, 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: GCJ)
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