ROBERT B. SCOTT PLASTIC ARTIFICAL
K-Number: K952538 · 1995-06-26
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Device Summary
Frequently Asked Questions
What is the ROBERT B. SCOTT PLASTIC ARTIFICAL?
ROBERT B. SCOTT PLASTIC ARTIFICAL is a medical device that received FDA 510(k) clearance on 1995-06-26. The listed applicant is Robert B. Scott Ocularists of Florida, Inc.. The 510(k) number is K952538.
When did ROBERT B. SCOTT PLASTIC ARTIFICAL receive FDA 510(k) clearance?
ROBERT B. SCOTT PLASTIC ARTIFICAL received FDA 510(k) clearance on 1995-06-26, under 510(k) number K952538.
Who is the listed applicant for ROBERT B. SCOTT PLASTIC ARTIFICAL?
The FDA 510(k) record lists Robert B. Scott Ocularists of Florida, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ROBERT B. SCOTT PLASTIC ARTIFICAL?
The FDA product code for ROBERT B. SCOTT PLASTIC ARTIFICAL is HQH.
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 Robert B. Scott Ocularists of Florida, 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: HQH)
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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