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FDA 510(k)

MAMIYA SLIT LAMP P-1

K-Number: K843099 · 1984-11-21

ApplicantOkada Corp.
Decision Date1984-11-21
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MAMIYA SLIT LAMP P-1 is the device name listed in this FDA 510(k) record. The listed applicant is Okada Corp.. It received FDA 510(k) clearance on 1984-11-21 under 510(k) number K843099. The device is classified under product code HLI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAMIYA SLIT LAMP P-1?

MAMIYA SLIT LAMP P-1 is a medical device that received FDA 510(k) clearance on 1984-11-21. The listed applicant is Okada Corp.. The 510(k) number is K843099.

When did MAMIYA SLIT LAMP P-1 receive FDA 510(k) clearance?

MAMIYA SLIT LAMP P-1 received FDA 510(k) clearance on 1984-11-21, under 510(k) number K843099.

Who is the listed applicant for MAMIYA SLIT LAMP P-1?

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

What is the FDA product code for MAMIYA SLIT LAMP P-1?

The FDA product code for MAMIYA SLIT LAMP P-1 is HLI.

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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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