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FDA 510(k)

QUANTUMATIC DUAL-WAVELENGTH SPECTRO

K-Number: K812865 · 1981-11-10

ApplicantAbbott Laboratories
Decision Date1981-11-10
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTUMATIC DUAL-WAVELENGTH SPECTRO is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K812865. 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 QUANTUMATIC DUAL-WAVELENGTH SPECTRO?

QUANTUMATIC DUAL-WAVELENGTH SPECTRO is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Abbott Laboratories. The 510(k) number is K812865.

When did QUANTUMATIC DUAL-WAVELENGTH SPECTRO receive FDA 510(k) clearance?

QUANTUMATIC DUAL-WAVELENGTH SPECTRO received FDA 510(k) clearance on 1981-11-10, under 510(k) number K812865.

Who is the listed applicant for QUANTUMATIC DUAL-WAVELENGTH SPECTRO?

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

What is the FDA product code for QUANTUMATIC DUAL-WAVELENGTH SPECTRO?

The FDA product code for QUANTUMATIC DUAL-WAVELENGTH SPECTRO is JJQ.

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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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