VIEWER, FLUOROMETIC, MODEL 721
K-Number: K770662 · 1977-04-15
Advertisement
Device Summary
Frequently Asked Questions
What is the VIEWER, FLUOROMETIC, MODEL 721?
VIEWER, FLUOROMETIC, MODEL 721 is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Corning Medical & Scientific. The 510(k) number is K770662.
When did VIEWER, FLUOROMETIC, MODEL 721 receive FDA 510(k) clearance?
VIEWER, FLUOROMETIC, MODEL 721 received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770662.
Who is the listed applicant for VIEWER, FLUOROMETIC, MODEL 721?
The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VIEWER, FLUOROMETIC, MODEL 721?
The FDA product code for VIEWER, FLUOROMETIC, MODEL 721 is JZT.
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 Corning Medical & Scientific 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: JZT)
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.
Advertisement