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FDA 510(k)

RECORDER, DINMAP, MODEL 950

K-Number: K771932 · 1977-11-07

ApplicantApplied Medical Research
Decision Date1977-11-07
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECORDER, DINMAP, MODEL 950 is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Research. It received FDA 510(k) clearance on 1977-11-07 under 510(k) number K771932. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECORDER, DINMAP, MODEL 950?

RECORDER, DINMAP, MODEL 950 is a medical device that received FDA 510(k) clearance on 1977-11-07. The listed applicant is Applied Medical Research. The 510(k) number is K771932.

When did RECORDER, DINMAP, MODEL 950 receive FDA 510(k) clearance?

RECORDER, DINMAP, MODEL 950 received FDA 510(k) clearance on 1977-11-07, under 510(k) number K771932.

Who is the listed applicant for RECORDER, DINMAP, MODEL 950?

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

What is the FDA product code for RECORDER, DINMAP, MODEL 950?

The FDA product code for RECORDER, DINMAP, MODEL 950 is DSH.

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Other records listing Applied Medical Research as applicant

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Related Devices (Code: DSH)

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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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