FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE
K-Number: K915857 · 1994-03-11
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Device Summary
Frequently Asked Questions
What is the FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE?
FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Olympus Corp.. The 510(k) number is K915857.
When did FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE receive FDA 510(k) clearance?
FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE received FDA 510(k) clearance on 1994-03-11, under 510(k) number K915857.
Who is the listed applicant for FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE?
The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE?
The FDA product code for FLEXIBLE TIP THORACOSCOPE/LAPAROSCOPE 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 Olympus 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: 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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