CANNULA, W/SHARP OBTURATOR & VERESS NEED
K-Number: K800668 · 1980-05-08
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Device Summary
Frequently Asked Questions
What is the CANNULA, W/SHARP OBTURATOR & VERESS NEED?
CANNULA, W/SHARP OBTURATOR & VERESS NEED is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K800668.
When did CANNULA, W/SHARP OBTURATOR & VERESS NEED receive FDA 510(k) clearance?
CANNULA, W/SHARP OBTURATOR & VERESS NEED received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800668.
Who is the listed applicant for CANNULA, W/SHARP OBTURATOR & VERESS NEED?
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 CANNULA, W/SHARP OBTURATOR & VERESS NEED?
The FDA product code for CANNULA, W/SHARP OBTURATOR & VERESS NEED is HET.
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 KARL STORZ Endoscopy-America, 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: HET)
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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