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FDA 510(k)

PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH

K-Number: K832374 · 1983-12-01

ApplicantSonicaid, Inc.
Decision Date1983-12-01
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1983-12-01 under 510(k) number K832374. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH?

PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH is a medical device that received FDA 510(k) clearance on 1983-12-01. The listed applicant is Sonicaid, Inc.. The 510(k) number is K832374.

When did PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH receive FDA 510(k) clearance?

PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH received FDA 510(k) clearance on 1983-12-01, under 510(k) number K832374.

Who is the listed applicant for PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH?

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

What is the FDA product code for PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH?

The FDA product code for PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH is JOM.

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Other records listing Sonicaid, Inc. as applicant

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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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