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FDA 510(k)

FORECASTER

K-Number: K810832 · 1981-06-24

ApplicantForecaster Co.
Decision Date1981-06-24
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

FORECASTER is the device name listed in this FDA 510(k) record. The listed applicant is Forecaster Co.. It received FDA 510(k) clearance on 1981-06-24 under 510(k) number K810832. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORECASTER?

FORECASTER is a medical device that received FDA 510(k) clearance on 1981-06-24. The listed applicant is Forecaster Co.. The 510(k) number is K810832.

When did FORECASTER receive FDA 510(k) clearance?

FORECASTER received FDA 510(k) clearance on 1981-06-24, under 510(k) number K810832.

Who is the listed applicant for FORECASTER?

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

What is the FDA product code for FORECASTER?

The FDA product code for FORECASTER is LHD.

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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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