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FDA 510(k)

TITERTEK MULTISKAN MCC

K-Number: K844418 · 1985-03-21

ApplicantFlow Laboratories, Inc.
Decision Date1985-03-21
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TITERTEK MULTISKAN MCC is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1985-03-21 under 510(k) number K844418. 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 TITERTEK MULTISKAN MCC?

TITERTEK MULTISKAN MCC is a medical device that received FDA 510(k) clearance on 1985-03-21. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K844418.

When did TITERTEK MULTISKAN MCC receive FDA 510(k) clearance?

TITERTEK MULTISKAN MCC received FDA 510(k) clearance on 1985-03-21, under 510(k) number K844418.

Who is the listed applicant for TITERTEK MULTISKAN MCC?

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

What is the FDA product code for TITERTEK MULTISKAN MCC?

The FDA product code for TITERTEK MULTISKAN MCC is JJQ.

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Other records listing Flow Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K861897UNISKAN IIK862066TITERTEK MICROPLATE WASHER S-12K861824GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)K861823GENTAMICIN SULFATE SOLUTION (50MG GENTAMICIN)K861791PENICILLIN-STREPTOMYCIN-FUNGIZONEK860762GAMMA-FREE HORSE SERUM

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Related Devices (Code: JJQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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