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FDA 510(k)

APLICARE SKIN PROTECTANT PREP PAD

K-Number: K861557 · 1986-07-11

Decision Date1986-07-11
Product CodeNEC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

APLICARE SKIN PROTECTANT PREP PAD is the device name listed in this FDA 510(k) record. The listed applicant is Aplicare, Inc.. It received FDA 510(k) clearance on 1986-07-11 under 510(k) number K861557. The device is classified under product code NEC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APLICARE SKIN PROTECTANT PREP PAD?

APLICARE SKIN PROTECTANT PREP PAD is a medical device that received FDA 510(k) clearance on 1986-07-11. The listed applicant is Aplicare, Inc.. The 510(k) number is K861557.

When did APLICARE SKIN PROTECTANT PREP PAD receive FDA 510(k) clearance?

APLICARE SKIN PROTECTANT PREP PAD received FDA 510(k) clearance on 1986-07-11, under 510(k) number K861557.

Who is the listed applicant for APLICARE SKIN PROTECTANT PREP PAD?

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

What is the FDA product code for APLICARE SKIN PROTECTANT PREP PAD?

The FDA product code for APLICARE SKIN PROTECTANT PREP PAD is NEC.

Related Clinical Trials

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.

Other records listing Aplicare, 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.

View all 9 devices →

Related Devices (Code: NEC)

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.

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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