FDA 510(k)

DUAL WAVELENGTH PHOTOMETER, 1177

K-Number: K771909 · 1977-12-20

Decision Date1977-12-20

Product CodeJJQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DUAL WAVELENGTH PHOTOMETER, 1177 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K771909. 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 DUAL WAVELENGTH PHOTOMETER, 1177?

DUAL WAVELENGTH PHOTOMETER, 1177 is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Abbott Laboratories. The 510(k) number is K771909.

When did DUAL WAVELENGTH PHOTOMETER, 1177 receive FDA 510(k) clearance?

DUAL WAVELENGTH PHOTOMETER, 1177 received FDA 510(k) clearance on 1977-12-20, under 510(k) number K771909.

Who is the listed applicant for DUAL WAVELENGTH PHOTOMETER, 1177?

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 DUAL WAVELENGTH PHOTOMETER, 1177?

The FDA product code for DUAL WAVELENGTH PHOTOMETER, 1177 is JJQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.