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FDA 510(k)

PHOTRON VISUAL FIELD ANALYZER

K-Number: K860642 · 1986-04-15

ApplicantBiosan Laboratories, Inc.
Decision Date1986-04-15
Product CodeHOM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PHOTRON VISUAL FIELD ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Biosan Laboratories, Inc.. It received FDA 510(k) clearance on 1986-04-15 under 510(k) number K860642. The device is classified under product code HOM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTRON VISUAL FIELD ANALYZER?

PHOTRON VISUAL FIELD ANALYZER is a medical device that received FDA 510(k) clearance on 1986-04-15. The listed applicant is Biosan Laboratories, Inc.. The 510(k) number is K860642.

When did PHOTRON VISUAL FIELD ANALYZER receive FDA 510(k) clearance?

PHOTRON VISUAL FIELD ANALYZER received FDA 510(k) clearance on 1986-04-15, under 510(k) number K860642.

Who is the listed applicant for PHOTRON VISUAL FIELD ANALYZER?

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

What is the FDA product code for PHOTRON VISUAL FIELD ANALYZER?

The FDA product code for PHOTRON VISUAL FIELD ANALYZER is HOM.

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Other records listing Biosan Laboratories, 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.

K853812PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)K832763TOBRAMYCIN REAGENTK833193RADIOIMMUNOASSAY, THYROID STIMU. HORMONEK834023BIO-SCIENCE LABORATORIES T4 REAGENTK833318NORMAL GOAT SERUMK833191ABNORMAL URINE CONTROL

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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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