BOBES TONOMETER
K-Number: K945446 · 1995-06-20
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Device Summary
Frequently Asked Questions
What is the BOBES TONOMETER?
BOBES TONOMETER is a medical device that received FDA 510(k) clearance on 1995-06-20. The listed applicant is Bobes S.A.. The 510(k) number is K945446.
When did BOBES TONOMETER receive FDA 510(k) clearance?
BOBES TONOMETER received FDA 510(k) clearance on 1995-06-20, under 510(k) number K945446.
Who is the listed applicant for BOBES TONOMETER?
The FDA 510(k) record lists Bobes S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOBES TONOMETER?
The FDA product code for BOBES TONOMETER is HKY.
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 Bobes S.A. 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: HKY)
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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