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FDA 510(k)

MULTISCRIPTOR EK 36/101 047 02,05

K-Number: K832130 · 1983-10-31

ApplicantLitton Medical Electronics
Decision Date1983-10-31
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MULTISCRIPTOR EK 36/101 047 02,05 is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K832130. 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 MULTISCRIPTOR EK 36/101 047 02,05?

MULTISCRIPTOR EK 36/101 047 02,05 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Litton Medical Electronics. The 510(k) number is K832130.

When did MULTISCRIPTOR EK 36/101 047 02,05 receive FDA 510(k) clearance?

MULTISCRIPTOR EK 36/101 047 02,05 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832130.

Who is the listed applicant for MULTISCRIPTOR EK 36/101 047 02,05?

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

What is the FDA product code for MULTISCRIPTOR EK 36/101 047 02,05?

The FDA product code for MULTISCRIPTOR EK 36/101 047 02,05 is DPS.

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Other records listing Litton Medical Electronics as applicant

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.

K840522RECOMED BLOOD-FLOW METER H236-052-02K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840439RECOMED CARDIAC OUTPUT METER 236067-K840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840209SERVOMED MEDIVISION SCOPE SMV-235

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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

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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