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FDA 510(k)

LIFELINE AMBULATORY

K-Number: K781054 · 1978-07-27

ApplicantImc
Decision Date1978-07-27
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFELINE AMBULATORY is the device name listed in this FDA 510(k) record. The listed applicant is Imc. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K781054. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFELINE AMBULATORY?

LIFELINE AMBULATORY is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Imc. The 510(k) number is K781054.

When did LIFELINE AMBULATORY receive FDA 510(k) clearance?

LIFELINE AMBULATORY received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781054.

Who is the listed applicant for LIFELINE AMBULATORY?

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

What is the FDA product code for LIFELINE AMBULATORY?

The FDA product code for LIFELINE AMBULATORY is DPS.

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Related Devices (Code: DPS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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