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FDA 510(k)

FLUSH SOLUTION CONCENTRATE

K-Number: K831020 · 1983-05-09

ApplicantFisher Scientific Co., LLC
Decision Date1983-05-09
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLUSH SOLUTION CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K831020. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUSH SOLUTION CONCENTRATE?

FLUSH SOLUTION CONCENTRATE is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K831020.

When did FLUSH SOLUTION CONCENTRATE receive FDA 510(k) clearance?

FLUSH SOLUTION CONCENTRATE received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831020.

Who is the listed applicant for FLUSH SOLUTION CONCENTRATE?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUSH SOLUTION CONCENTRATE?

The FDA product code for FLUSH SOLUTION CONCENTRATE is CHL.

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Other records listing Fisher Scientific Co., LLC 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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