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FDA 510(k)

MODEL 690 SPECTROPHOTOMETER

K-Number: K873408 · 1987-09-08

ApplicantAbbott Diagnostics
Decision Date1987-09-08
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 690 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 1987-09-08 under 510(k) number K873408. 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 690 SPECTROPHOTOMETER?

MODEL 690 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1987-09-08. The listed applicant is Abbott Diagnostics. The 510(k) number is K873408.

When did MODEL 690 SPECTROPHOTOMETER receive FDA 510(k) clearance?

MODEL 690 SPECTROPHOTOMETER received FDA 510(k) clearance on 1987-09-08, under 510(k) number K873408.

Who is the listed applicant for MODEL 690 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 690 SPECTROPHOTOMETER?

The FDA product code for MODEL 690 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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