DIGITAL SCANNER
K-Number: K770526 · 1977-04-08
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Device Summary
Frequently Asked Questions
What is the DIGITAL SCANNER?
DIGITAL SCANNER is a medical device that received FDA 510(k) clearance on 1977-04-08. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K770526.
When did DIGITAL SCANNER receive FDA 510(k) clearance?
DIGITAL SCANNER received FDA 510(k) clearance on 1977-04-08, under 510(k) number K770526.
Who is the listed applicant for DIGITAL SCANNER?
The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL SCANNER?
The FDA product code for DIGITAL SCANNER is JXR.
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 The Perkin-Elmer 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: JXR)
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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