GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM
K-Number: K900958 · 1990-04-18
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Device Summary
Frequently Asked Questions
What is the GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM?
GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM is a medical device that received FDA 510(k) clearance on 1990-04-18. The listed applicant is Solos Endoscopy, Inc.. The 510(k) number is K900958.
When did GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM receive FDA 510(k) clearance?
GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM received FDA 510(k) clearance on 1990-04-18, under 510(k) number K900958.
Who is the listed applicant for GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM?
The FDA 510(k) record lists Solos Endoscopy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM?
The FDA product code for GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MM is GEJ.
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 Solos Endoscopy, 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: GEJ)
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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