REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS
K-Number: K022748 · 2002-10-09
Advertisement
Device Summary
Frequently Asked Questions
What is the REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?
REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is a medical device that received FDA 510(k) clearance on 2002-10-09. The listed applicant is Medical Device Services. The 510(k) number is K022748.
When did REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS receive FDA 510(k) clearance?
REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS received FDA 510(k) clearance on 2002-10-09, under 510(k) number K022748.
Who is the listed applicant for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?
The FDA 510(k) record lists Medical Device Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS?
The FDA product code for REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS is HET.
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 Medical Device Services 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: HET)
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