SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA
K-Number: K910985 · 1991-07-05
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Device Summary
Frequently Asked Questions
What is the SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?
SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA is a medical device that received FDA 510(k) clearance on 1991-07-05. The listed applicant is Precision Laser Products, Inc.. The 510(k) number is K910985.
When did SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA receive FDA 510(k) clearance?
SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA received FDA 510(k) clearance on 1991-07-05, under 510(k) number K910985.
Who is the listed applicant for SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?
The FDA 510(k) record lists Precision Laser Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA?
The FDA product code for SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA 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 Precision Laser Products, 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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