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FDA 510(k)

SYRINGE TONOMETER

K-Number: K790803 · 1979-06-28

ApplicantMedicor USA , Ltd.
Decision Date1979-06-28
Product Code
DecisionSubstantially Equivalent

Device Summary

SYRINGE TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K790803. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYRINGE TONOMETER?

SYRINGE TONOMETER is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K790803.

When did SYRINGE TONOMETER receive FDA 510(k) clearance?

SYRINGE TONOMETER received FDA 510(k) clearance on 1979-06-28, under 510(k) number K790803.

Who is the listed applicant for SYRINGE TONOMETER?

The FDA 510(k) record lists Medicor USA , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Medicor USA , Ltd. 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.

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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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