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FDA 510(k)

JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680

K-Number: K931878 · 1993-08-19

Decision Date1993-08-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JARIT ENDOSCOPES, 600-600; 600-630; 600-650; 680 is the device name listed in this FDA 510(k) record. The listed applicant is J. Jamner Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1993-08-19 under 510(k) number K931878. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 11 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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