FDA 510(k)

SHUR-LOCK ICE WRAP SYSTEM

K-Number: K904819 · 1990-12-06

Decision Date1990-12-06

Product CodeIMD

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

SHUR-LOCK ICE WRAP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Conco Medical Co.. It received FDA 510(k) clearance on 1990-12-06 under 510(k) number K904819. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHUR-LOCK ICE WRAP SYSTEM?

SHUR-LOCK ICE WRAP SYSTEM is a medical device that received FDA 510(k) clearance on 1990-12-06. The listed applicant is Conco Medical Co.. The 510(k) number is K904819.

When did SHUR-LOCK ICE WRAP SYSTEM receive FDA 510(k) clearance?

SHUR-LOCK ICE WRAP SYSTEM received FDA 510(k) clearance on 1990-12-06, under 510(k) number K904819.

Who is the listed applicant for SHUR-LOCK ICE WRAP SYSTEM?

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

What is the FDA product code for SHUR-LOCK ICE WRAP SYSTEM?

The FDA product code for SHUR-LOCK ICE WRAP SYSTEM is IMD.

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Other records listing Conco Medical Co. as applicant

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Related Devices (Code: IMD)

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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.