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FDA 510(k)

CONPHAR-SCHIOETZ TONOMETER

K-Number: K813619 · 1982-02-24

ApplicantConphar, Inc.
Decision Date1982-02-24
Product CodeHKY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONPHAR-SCHIOETZ TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-02-24 under 510(k) number K813619. The device is classified under product code HKY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONPHAR-SCHIOETZ TONOMETER?

CONPHAR-SCHIOETZ TONOMETER is a medical device that received FDA 510(k) clearance on 1982-02-24. The listed applicant is Conphar, Inc.. The 510(k) number is K813619.

When did CONPHAR-SCHIOETZ TONOMETER receive FDA 510(k) clearance?

CONPHAR-SCHIOETZ TONOMETER received FDA 510(k) clearance on 1982-02-24, under 510(k) number K813619.

Who is the listed applicant for CONPHAR-SCHIOETZ TONOMETER?

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

What is the FDA product code for CONPHAR-SCHIOETZ TONOMETER?

The FDA product code for CONPHAR-SCHIOETZ 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 Conphar, 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 122 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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