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FDA 510(k)

SIMPLISCRIPTOR EK 31/101 037 16

K-Number: K832184 · 1983-10-31

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

Device Summary

SIMPLISCRIPTOR EK 31/101 037 16 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 K832184. 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 SIMPLISCRIPTOR EK 31/101 037 16?

SIMPLISCRIPTOR EK 31/101 037 16 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 K832184.

When did SIMPLISCRIPTOR EK 31/101 037 16 receive FDA 510(k) clearance?

SIMPLISCRIPTOR EK 31/101 037 16 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832184.

Who is the listed applicant for SIMPLISCRIPTOR EK 31/101 037 16?

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 SIMPLISCRIPTOR EK 31/101 037 16?

The FDA product code for SIMPLISCRIPTOR EK 31/101 037 16 is DPS.

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Other records listing Litton Medical Electronics as applicant

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Related Devices (Code: DPS)

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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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