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FDA 510(k)

LIMB HOLDER, TECNOL REMINDER

K-Number: K760309 · 1976-08-09

ApplicantTecnol New Jersey Wound Care, Inc.
Decision Date1976-08-09
Product Code
DecisionSubstantially Equivalent

Device Summary

LIMB HOLDER, TECNOL REMINDER 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 1976-08-09 under 510(k) number K760309. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIMB HOLDER, TECNOL REMINDER?

LIMB HOLDER, TECNOL REMINDER is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K760309.

When did LIMB HOLDER, TECNOL REMINDER receive FDA 510(k) clearance?

LIMB HOLDER, TECNOL REMINDER received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760309.

Who is the listed applicant for LIMB HOLDER, TECNOL REMINDER?

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

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

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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