DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM
K-Number: K944162 · 1994-11-29
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Device Summary
Frequently Asked Questions
What is the DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM?
DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-11-29. The listed applicant is Teledyne Water Pik. The 510(k) number is K944162.
When did DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM receive FDA 510(k) clearance?
DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM received FDA 510(k) clearance on 1994-11-29, under 510(k) number K944162.
Who is the listed applicant for DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM?
The FDA 510(k) record lists Teledyne Water Pik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM?
The FDA product code for DENAR ACCUCEPH CEPHALOMETER IMAGING SYSTEM is EAG.
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 Teledyne Water Pik 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: EAG)
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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