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FDA 510(k)

HUMPHREY FIELD ANALYZER (HFA II)

K-Number: K954167 · 1995-11-24

Decision Date1995-11-24
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

HUMPHREY FIELD ANALYZER (HFA II) is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1995-11-24 under 510(k) number K954167. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMPHREY FIELD ANALYZER (HFA II)?

HUMPHREY FIELD ANALYZER (HFA II) is a medical device that received FDA 510(k) clearance on 1995-11-24. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K954167.

When did HUMPHREY FIELD ANALYZER (HFA II) receive FDA 510(k) clearance?

HUMPHREY FIELD ANALYZER (HFA II) received FDA 510(k) clearance on 1995-11-24, under 510(k) number K954167.

Who is the listed applicant for HUMPHREY FIELD ANALYZER (HFA II)?

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

What is the FDA product code for HUMPHREY FIELD ANALYZER (HFA II)?

The FDA product code for HUMPHREY FIELD ANALYZER (HFA II) is HPT.

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 Carl Zeiss, 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 44 devices →

Related Devices (Code: HPT)

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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