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FDA 510(k)

EBS 775 TONOMETER

K-Number: K781386 · 1978-09-14

Decision Date1978-09-14
Product CodeLCH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EBS 775 TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Equilibrated Bio Systems, Inc.. It received FDA 510(k) clearance on 1978-09-14 under 510(k) number K781386. The device is classified under product code LCH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBS 775 TONOMETER?

EBS 775 TONOMETER is a medical device that received FDA 510(k) clearance on 1978-09-14. The listed applicant is Equilibrated Bio Systems, Inc.. The 510(k) number is K781386.

When did EBS 775 TONOMETER receive FDA 510(k) clearance?

EBS 775 TONOMETER received FDA 510(k) clearance on 1978-09-14, under 510(k) number K781386.

Who is the listed applicant for EBS 775 TONOMETER?

The FDA 510(k) record lists Equilibrated Bio Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EBS 775 TONOMETER?

The FDA product code for EBS 775 TONOMETER is LCH.

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 Equilibrated Bio Systems, 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.

View all 7 devices →

Related Devices (Code: LCH)

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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