ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER)
K-Number: K042831 · 2004-10-28
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Device Summary
Frequently Asked Questions
What is the ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER)?
ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER) is a medical device that received FDA 510(k) clearance on 2004-10-28. The listed applicant is Reichert, Inc.. The 510(k) number is K042831.
When did ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER) receive FDA 510(k) clearance?
ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER) received FDA 510(k) clearance on 2004-10-28, under 510(k) number K042831.
Who is the listed applicant for ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER)?
The FDA 510(k) record lists Reichert, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER)?
The FDA product code for ATP (AUTO NON-CONTACT TONOMETER/PACHYMETER) is IYO.
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 Reichert, Inc. 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: IYO)
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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