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FDA 510(k)

STRIP SPLITTER II -HALF WIDTH CARRIER

K-Number: K834150 · 1984-01-11

ApplicantLarken Industries, Inc.
Decision Date1984-01-11
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

STRIP SPLITTER II -HALF WIDTH CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is Larken Industries, Inc.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K834150. 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 STRIP SPLITTER II -HALF WIDTH CARRIER?

STRIP SPLITTER II -HALF WIDTH CARRIER is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Larken Industries, Inc.. The 510(k) number is K834150.

When did STRIP SPLITTER II -HALF WIDTH CARRIER receive FDA 510(k) clearance?

STRIP SPLITTER II -HALF WIDTH CARRIER received FDA 510(k) clearance on 1984-01-11, under 510(k) number K834150.

Who is the listed applicant for STRIP SPLITTER II -HALF WIDTH CARRIER?

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

What is the FDA product code for STRIP SPLITTER II -HALF WIDTH CARRIER?

The FDA product code for STRIP SPLITTER II -HALF WIDTH CARRIER is JJQ.

Related Clinical Trials

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Other records listing Larken Industries, 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.

K871586GLUCOCHEK S.C. WITH AUDIO OPTIONK842474GLUCOCHEK III

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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