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FDA 510(k)

LINE CHARGER MODEL LC-100

K-Number: K772053 · 1977-11-09

ApplicantDatascope Corp.
Decision Date1977-11-09
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LINE CHARGER MODEL LC-100 is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1977-11-09 under 510(k) number K772053. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINE CHARGER MODEL LC-100?

LINE CHARGER MODEL LC-100 is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is Datascope Corp.. The 510(k) number is K772053.

When did LINE CHARGER MODEL LC-100 receive FDA 510(k) clearance?

LINE CHARGER MODEL LC-100 received FDA 510(k) clearance on 1977-11-09, under 510(k) number K772053.

Who is the listed applicant for LINE CHARGER MODEL LC-100?

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

What is the FDA product code for LINE CHARGER MODEL LC-100?

The FDA product code for LINE CHARGER MODEL LC-100 is DRT.

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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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