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FDA 510(k)

ULTROSPEC W/APPLE II -4050-

K-Number: K834489 · 1984-02-10

ApplicantLkb Instruments, Inc.
Decision Date1984-02-10
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTROSPEC W/APPLE II -4050- is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K834489. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTROSPEC W/APPLE II -4050-?

ULTROSPEC W/APPLE II -4050- is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K834489.

When did ULTROSPEC W/APPLE II -4050- receive FDA 510(k) clearance?

ULTROSPEC W/APPLE II -4050- received FDA 510(k) clearance on 1984-02-10, under 510(k) number K834489.

Who is the listed applicant for ULTROSPEC W/APPLE II -4050-?

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

What is the FDA product code for ULTROSPEC W/APPLE II -4050-?

The FDA product code for ULTROSPEC W/APPLE II -4050- is JJQ.

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Related Devices (Code: JJQ)

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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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