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FDA 510(k)

COMPRESSAR DISPOSABLE DISC

K-Number: K831337 · 1983-07-19

ApplicantInstromedix, Inc.
Decision Date1983-07-19
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COMPRESSAR DISPOSABLE DISC is the device name listed in this FDA 510(k) record. The listed applicant is Instromedix, Inc.. It received FDA 510(k) clearance on 1983-07-19 under 510(k) number K831337. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMPRESSAR DISPOSABLE DISC?

COMPRESSAR DISPOSABLE DISC is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is Instromedix, Inc.. The 510(k) number is K831337.

When did COMPRESSAR DISPOSABLE DISC receive FDA 510(k) clearance?

COMPRESSAR DISPOSABLE DISC received FDA 510(k) clearance on 1983-07-19, under 510(k) number K831337.

Who is the listed applicant for COMPRESSAR DISPOSABLE DISC?

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

What is the FDA product code for COMPRESSAR DISPOSABLE DISC?

The FDA product code for COMPRESSAR DISPOSABLE DISC is DQO.

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Related Devices (Code: DQO)

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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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