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FDA 510(k)

DIGILAB MICRO ONE APPLANATION TONOMETER

K-Number: K870121 · 1987-02-20

ApplicantBio-Rad
Decision Date1987-02-20
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DIGILAB MICRO ONE APPLANATION TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K870121. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGILAB MICRO ONE APPLANATION TONOMETER?

DIGILAB MICRO ONE APPLANATION TONOMETER is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Bio-Rad. The 510(k) number is K870121.

When did DIGILAB MICRO ONE APPLANATION TONOMETER receive FDA 510(k) clearance?

DIGILAB MICRO ONE APPLANATION TONOMETER received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870121.

Who is the listed applicant for DIGILAB MICRO ONE APPLANATION TONOMETER?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGILAB MICRO ONE APPLANATION TONOMETER?

The FDA product code for DIGILAB MICRO ONE APPLANATION TONOMETER is HKX.

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Related Devices (Code: HKX)

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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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