JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680
K-Number: K931878 · 1993-08-19
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Device Summary
Frequently Asked Questions
What is the JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680?
JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680 is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is J. Jamner Surgical Instruments, Inc.. The 510(k) number is K931878.
When did JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680 receive FDA 510(k) clearance?
JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680 received FDA 510(k) clearance on 1993-08-19, under 510(k) number K931878.
Who is the listed applicant for JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680?
The FDA 510(k) record lists J. Jamner Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680?
The FDA product code for JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680 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 J. Jamner 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: 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.
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