PANORAMIC X-RAY SYSTEM MODEL A
K-Number: K772164 · 1977-12-02
Advertisement
Device Summary
Frequently Asked Questions
What is the PANORAMIC X-RAY SYSTEM MODEL A?
PANORAMIC X-RAY SYSTEM MODEL A is a medical device that received FDA 510(k) clearance on 1977-12-02. The listed applicant is Sybron Corp.. The 510(k) number is K772164.
When did PANORAMIC X-RAY SYSTEM MODEL A receive FDA 510(k) clearance?
PANORAMIC X-RAY SYSTEM MODEL A received FDA 510(k) clearance on 1977-12-02, under 510(k) number K772164.
Who is the listed applicant for PANORAMIC X-RAY SYSTEM MODEL A?
The FDA 510(k) record lists Sybron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PANORAMIC X-RAY SYSTEM MODEL A?
The FDA product code for PANORAMIC X-RAY SYSTEM MODEL A is EHD.
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 Sybron 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: EHD)
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