LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS
K-Number: K971796 · 1997-08-12
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Device Summary
Frequently Asked Questions
What is the LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS?
LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS is a medical device that received FDA 510(k) clearance on 1997-08-12. The listed applicant is Louisville Laboratories, Inc.. The 510(k) number is K971796.
When did LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS receive FDA 510(k) clearance?
LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS received FDA 510(k) clearance on 1997-08-12, under 510(k) number K971796.
Who is the listed applicant for LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS?
The FDA 510(k) record lists Louisville Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS?
The FDA product code for LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS is EZL.
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 Louisville 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: EZL)
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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