NEOPROBE PORTABLE RADIOSCOPE DETECTOR
K-Number: K915279 · 1992-06-10
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Device Summary
Frequently Asked Questions
What is the NEOPROBE PORTABLE RADIOSCOPE DETECTOR?
NEOPROBE PORTABLE RADIOSCOPE DETECTOR is a medical device that received FDA 510(k) clearance on 1992-06-10. The listed applicant is Neoprobe Corp.. The 510(k) number is K915279.
When did NEOPROBE PORTABLE RADIOSCOPE DETECTOR receive FDA 510(k) clearance?
NEOPROBE PORTABLE RADIOSCOPE DETECTOR received FDA 510(k) clearance on 1992-06-10, under 510(k) number K915279.
Who is the listed applicant for NEOPROBE PORTABLE RADIOSCOPE DETECTOR?
The FDA 510(k) record lists Neoprobe Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEOPROBE PORTABLE RADIOSCOPE DETECTOR?
The FDA product code for NEOPROBE PORTABLE RADIOSCOPE DETECTOR is IZD.
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 Neoprobe 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: IZD)
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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