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FDA 510(k)

MODEL 340 SPECTROPHOTOMETER

K-Number: K822720 · 1982-10-08

ApplicantAbbott Diagnostics
Decision Date1982-10-08
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 340 SPECTROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Diagnostics. It received FDA 510(k) clearance on 1982-10-08 under 510(k) number K822720. 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 MODEL 340 SPECTROPHOTOMETER?

MODEL 340 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1982-10-08. The listed applicant is Abbott Diagnostics. The 510(k) number is K822720.

When did MODEL 340 SPECTROPHOTOMETER receive FDA 510(k) clearance?

MODEL 340 SPECTROPHOTOMETER received FDA 510(k) clearance on 1982-10-08, under 510(k) number K822720.

Who is the listed applicant for MODEL 340 SPECTROPHOTOMETER?

The FDA 510(k) record lists Abbott Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 340 SPECTROPHOTOMETER?

The FDA product code for MODEL 340 SPECTROPHOTOMETER is JJQ.

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Other records listing Abbott Diagnostics 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.

K964185IMX CA 125K972182ABBOTT STREP A CONTROLSK961439ABBOTT CELL-DYN 4000 SYSTEMK890491CELL-DYN 3000 MULTI-PARAMETER HEMATOLOGY ANALYERK881242CELL-DYN RAPID-LYSE AND HEMOGLOBLINK881130CELL-DYN ISOTONIC DILUENT

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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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