REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING
K-Number: K930571 · 1994-02-01
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Device Summary
Frequently Asked Questions
What is the REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING?
REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Numed Technologies, Inc.. The 510(k) number is K930571.
When did REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING receive FDA 510(k) clearance?
REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING received FDA 510(k) clearance on 1994-02-01, under 510(k) number K930571.
Who is the listed applicant for REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING?
The FDA 510(k) record lists Numed Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING?
The FDA product code for REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATING is HFI.
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 Numed Technologies, 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: HFI)
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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