Decision Date1995-04-05
Product CodeKOC
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-04-05 under 510(k) number K950282. The device is classified under product code KOC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA?
KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA is a medical device that received FDA 510(k) clearance on 1995-04-05. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K950282.
When did KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA receive FDA 510(k) clearance?
KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA received FDA 510(k) clearance on 1995-04-05, under 510(k) number K950282.
Who is the listed applicant for KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA?
The FDA product code for KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA is KOC.
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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.