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FDA 510(k)

DISPOSABLE DIAPHRAGM DONE

K-Number: K803011 · 1980-12-31

ApplicantSorensen Research
Decision Date1980-12-31
Product CodeDRQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE DIAPHRAGM DONE is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1980-12-31 under 510(k) number K803011. The device is classified under product code DRQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE DIAPHRAGM DONE?

DISPOSABLE DIAPHRAGM DONE is a medical device that received FDA 510(k) clearance on 1980-12-31. The listed applicant is Sorensen Research. The 510(k) number is K803011.

When did DISPOSABLE DIAPHRAGM DONE receive FDA 510(k) clearance?

DISPOSABLE DIAPHRAGM DONE received FDA 510(k) clearance on 1980-12-31, under 510(k) number K803011.

Who is the listed applicant for DISPOSABLE DIAPHRAGM DONE?

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

What is the FDA product code for DISPOSABLE DIAPHRAGM DONE?

The FDA product code for DISPOSABLE DIAPHRAGM DONE is DRQ.

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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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