MENTOR INJECTION PORT DETECTOR (IPD)
K-Number: K963066 · 1996-09-27
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Device Summary
Frequently Asked Questions
What is the MENTOR INJECTION PORT DETECTOR (IPD)?
MENTOR INJECTION PORT DETECTOR (IPD) is a medical device that received FDA 510(k) clearance on 1996-09-27. The listed applicant is Mentor Corp.. The 510(k) number is K963066.
When did MENTOR INJECTION PORT DETECTOR (IPD) receive FDA 510(k) clearance?
MENTOR INJECTION PORT DETECTOR (IPD) received FDA 510(k) clearance on 1996-09-27, under 510(k) number K963066.
Who is the listed applicant for MENTOR INJECTION PORT DETECTOR (IPD)?
The FDA 510(k) record lists Mentor Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MENTOR INJECTION PORT DETECTOR (IPD)?
The FDA product code for MENTOR INJECTION PORT DETECTOR (IPD) is LCJ.
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 Mentor 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: LCJ)
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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