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FDA 510(k)

SHELF LIFE CHANGE OF STERILE DEVICES

K-Number: K864090 · 1987-03-20

ApplicantUtah Medical Products, Inc.
Decision Date1987-03-20
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SHELF LIFE CHANGE OF STERILE DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Utah Medical Products, Inc.. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K864090. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHELF LIFE CHANGE OF STERILE DEVICES?

SHELF LIFE CHANGE OF STERILE DEVICES is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K864090.

When did SHELF LIFE CHANGE OF STERILE DEVICES receive FDA 510(k) clearance?

SHELF LIFE CHANGE OF STERILE DEVICES received FDA 510(k) clearance on 1987-03-20, under 510(k) number K864090.

Who is the listed applicant for SHELF LIFE CHANGE OF STERILE DEVICES?

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

What is the FDA product code for SHELF LIFE CHANGE OF STERILE DEVICES?

The FDA product code for SHELF LIFE CHANGE OF STERILE DEVICES is DRS.

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Other records listing Utah Medical Products, 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.

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