NUCLEAR ASSOCIATES GLASSERS
K-Number: K934362 · 1993-11-12
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Device Summary
Frequently Asked Questions
What is the NUCLEAR ASSOCIATES GLASSERS?
NUCLEAR ASSOCIATES GLASSERS is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Victoreen, Inc.. The 510(k) number is K934362.
When did NUCLEAR ASSOCIATES GLASSERS receive FDA 510(k) clearance?
NUCLEAR ASSOCIATES GLASSERS received FDA 510(k) clearance on 1993-11-12, under 510(k) number K934362.
Who is the listed applicant for NUCLEAR ASSOCIATES GLASSERS?
The FDA 510(k) record lists Victoreen, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NUCLEAR ASSOCIATES GLASSERS?
The FDA product code for NUCLEAR ASSOCIATES GLASSERS is IWS.
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 Victoreen, 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: IWS)
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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