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FDA 510(k)

TELEMETRY, BIOMEDICAL

K-Number: K790109 · 1979-03-16

ApplicantLkc Technologies, Inc.
Decision Date1979-03-16
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELEMETRY, BIOMEDICAL is the device name listed in this FDA 510(k) record. The listed applicant is Lkc Technologies, Inc.. It received FDA 510(k) clearance on 1979-03-16 under 510(k) number K790109. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEMETRY, BIOMEDICAL?

TELEMETRY, BIOMEDICAL is a medical device that received FDA 510(k) clearance on 1979-03-16. The listed applicant is Lkc Technologies, Inc.. The 510(k) number is K790109.

When did TELEMETRY, BIOMEDICAL receive FDA 510(k) clearance?

TELEMETRY, BIOMEDICAL received FDA 510(k) clearance on 1979-03-16, under 510(k) number K790109.

Who is the listed applicant for TELEMETRY, BIOMEDICAL?

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

What is the FDA product code for TELEMETRY, BIOMEDICAL?

The FDA product code for TELEMETRY, BIOMEDICAL is DRG.

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Other records listing Lkc Technologies, 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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