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FDA 510(k)

TECNOL PATIENT USE ICE PACK

K-Number: K760782 · 1976-12-02

ApplicantTecnol New Jersey Wound Care, Inc.
Decision Date1976-12-02
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TECNOL PATIENT USE ICE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1976-12-02 under 510(k) number K760782. 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 TECNOL PATIENT USE ICE PACK?

TECNOL PATIENT USE ICE PACK is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K760782.

When did TECNOL PATIENT USE ICE PACK receive FDA 510(k) clearance?

TECNOL PATIENT USE ICE PACK received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760782.

Who is the listed applicant for TECNOL PATIENT USE ICE PACK?

The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECNOL PATIENT USE ICE PACK?

The FDA product code for TECNOL PATIENT USE ICE PACK is ILO.

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Other records listing Tecnol New Jersey Wound Care, Inc. as applicant

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Related Devices (Code: 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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