LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM
K-Number: K930569 · 1993-04-20
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Device Summary
Frequently Asked Questions
What is the LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM?
LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Laparomed Corp.. The 510(k) number is K930569.
When did LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM receive FDA 510(k) clearance?
LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM received FDA 510(k) clearance on 1993-04-20, under 510(k) number K930569.
Who is the listed applicant for LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM?
The FDA 510(k) record lists Laparomed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM?
The FDA product code for LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM 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 Laparomed Corp. 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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