PROPHY ANGLES, R&R
K-Number: K780199 · 1978-02-16
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Device Summary
Frequently Asked Questions
What is the PROPHY ANGLES, R&R?
PROPHY ANGLES, R&R is a medical device that received FDA 510(k) clearance on 1978-02-16. The listed applicant is Ransom and Randolph. The 510(k) number is K780199.
When did PROPHY ANGLES, R&R receive FDA 510(k) clearance?
PROPHY ANGLES, R&R received FDA 510(k) clearance on 1978-02-16, under 510(k) number K780199.
Who is the listed applicant for PROPHY ANGLES, R&R?
The FDA 510(k) record lists Ransom and Randolph as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROPHY ANGLES, R&R?
The FDA product code for PROPHY ANGLES, R&R is EGS.
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 Ransom and Randolph 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: EGS)
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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