FDA 510(k)

CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90

K-Number: K853072 · 1985-12-09

Decision Date1985-12-09

Product CodeDYB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90 is the device name listed in this FDA 510(k) record. The listed applicant is Camino Laboratories, Inc.. It received FDA 510(k) clearance on 1985-12-09 under 510(k) number K853072. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90?

CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90 is a medical device that received FDA 510(k) clearance on 1985-12-09. The listed applicant is Camino Laboratories, Inc.. The 510(k) number is K853072.

When did CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90 receive FDA 510(k) clearance?

CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90 received FDA 510(k) clearance on 1985-12-09, under 510(k) number K853072.

Who is the listed applicant for CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90?

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

What is the FDA product code for CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90?

The FDA product code for CORON PRES MONITOR KIT MODEL 80 LEFT KIT MODEL 90 is DYB.

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Other records listing Camino Laboratories, Inc. as applicant

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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.