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FDA 510(k)

KEELER KONAN SPECULAR MICROSCOPE SP3300

K-Number: K900111 · 1990-03-23

ApplicantKeeler Instruments, Inc.
Decision Date1990-03-23
Product CodeHLI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KEELER KONAN SPECULAR MICROSCOPE SP3300 is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1990-03-23 under 510(k) number K900111. 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 KEELER KONAN SPECULAR MICROSCOPE SP3300?

KEELER KONAN SPECULAR MICROSCOPE SP3300 is a medical device that received FDA 510(k) clearance on 1990-03-23. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K900111.

When did KEELER KONAN SPECULAR MICROSCOPE SP3300 receive FDA 510(k) clearance?

KEELER KONAN SPECULAR MICROSCOPE SP3300 received FDA 510(k) clearance on 1990-03-23, under 510(k) number K900111.

Who is the listed applicant for KEELER KONAN SPECULAR MICROSCOPE SP3300?

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

What is the FDA product code for KEELER KONAN SPECULAR MICROSCOPE SP3300?

The FDA product code for KEELER KONAN SPECULAR MICROSCOPE SP3300 is HLI.

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Other records listing Keeler Instruments, Inc. as applicant

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Related Devices (Code: HLI)

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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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