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FDA 510(k)

BUFFER PACK FOR ABL-1 & ABL-2

K-Number: K831017 · 1983-05-09

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

Device Summary

BUFFER PACK FOR ABL-1 & ABL-2 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 K831017. 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 BUFFER PACK FOR ABL-1 & ABL-2?

BUFFER PACK FOR ABL-1 & ABL-2 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 K831017.

When did BUFFER PACK FOR ABL-1 & ABL-2 receive FDA 510(k) clearance?

BUFFER PACK FOR ABL-1 & ABL-2 received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831017.

Who is the listed applicant for BUFFER PACK FOR ABL-1 & ABL-2?

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 BUFFER PACK FOR ABL-1 & ABL-2?

The FDA product code for BUFFER PACK FOR ABL-1 & ABL-2 is CHL.

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Other records listing Fisher Scientific Co., LLC as applicant

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K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: CHL)

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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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