Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CANON 60 DEGREE FUNDUS CAMERA CF-60S

K-Number: K844053 · 1984-12-19

Decision Date1984-12-19
Product CodeHFI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CANON 60 DEGREE FUNDUS CAMERA CF-60S is the device name listed in this FDA 510(k) record. The listed applicant is Canon USA, Inc.. It received FDA 510(k) clearance on 1984-12-19 under 510(k) number K844053. The device is classified under product code HFI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANON 60 DEGREE FUNDUS CAMERA CF-60S?

CANON 60 DEGREE FUNDUS CAMERA CF-60S is a medical device that received FDA 510(k) clearance on 1984-12-19. The listed applicant is Canon USA, Inc.. The 510(k) number is K844053.

When did CANON 60 DEGREE FUNDUS CAMERA CF-60S receive FDA 510(k) clearance?

CANON 60 DEGREE FUNDUS CAMERA CF-60S received FDA 510(k) clearance on 1984-12-19, under 510(k) number K844053.

Who is the listed applicant for CANON 60 DEGREE FUNDUS CAMERA CF-60S?

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

What is the FDA product code for CANON 60 DEGREE FUNDUS CAMERA CF-60S?

The FDA product code for CANON 60 DEGREE FUNDUS CAMERA CF-60S is HFI.

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 Canon USA, 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 48 devices →

Related Devices (Code: HFI)

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

View on FDA Database →

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

↑