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FDA 510(k)

HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS

K-Number: K931843 · 1994-02-02

ApplicantHollister, Inc.
Decision Date1994-02-02
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1994-02-02 under 510(k) number K931843. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS?

HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Hollister, Inc.. The 510(k) number is K931843.

When did HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS receive FDA 510(k) clearance?

HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS received FDA 510(k) clearance on 1994-02-02, under 510(k) number K931843.

Who is the listed applicant for HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS?

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

What is the FDA product code for HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS?

The FDA product code for HOT/ICE SYSTEM STERILE CONFORMABLE/DISP. BLANKETS is ILO.

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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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