LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS
K-Number: K955845 · 1996-07-05
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Device Summary
Frequently Asked Questions
What is the LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS?
LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS is a medical device that received FDA 510(k) clearance on 1996-07-05. The listed applicant is Surgical Image Laboratories, Inc.. The 510(k) number is K955845.
When did LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS receive FDA 510(k) clearance?
LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS received FDA 510(k) clearance on 1996-07-05, under 510(k) number K955845.
Who is the listed applicant for LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS?
The FDA 510(k) record lists Surgical Image Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS?
The FDA product code for LL 100, 103, 104 DIAGNOSTIC LAPAROSCOPE RIGID ROD LENS 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 Surgical Image Laboratories, 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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