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FDA 510(k)

'MICROLYTE 4/5'

K-Number: K873345 · 1987-09-11

ApplicantKone Instruments, Inc.
Decision Date1987-09-11
Product CodeJFP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

'MICROLYTE 4/5' is the device name listed in this FDA 510(k) record. The listed applicant is Kone Instruments, Inc.. It received FDA 510(k) clearance on 1987-09-11 under 510(k) number K873345. The device is classified under product code JFP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 'MICROLYTE 4/5'?

'MICROLYTE 4/5' is a medical device that received FDA 510(k) clearance on 1987-09-11. The listed applicant is Kone Instruments, Inc.. The 510(k) number is K873345.

When did 'MICROLYTE 4/5' receive FDA 510(k) clearance?

'MICROLYTE 4/5' received FDA 510(k) clearance on 1987-09-11, under 510(k) number K873345.

Who is the listed applicant for 'MICROLYTE 4/5'?

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

What is the FDA product code for 'MICROLYTE 4/5'?

The FDA product code for 'MICROLYTE 4/5' is JFP.

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Other records listing Kone Instruments, Inc. as applicant

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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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