KIT PAK INCONTINENT SKIN CARE KIT
K-Number: K932310 · 1994-06-01
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Device Summary
Frequently Asked Questions
What is the KIT PAK INCONTINENT SKIN CARE KIT?
KIT PAK INCONTINENT SKIN CARE KIT is a medical device that received FDA 510(k) clearance on 1994-06-01. The listed applicant is Kit Pak, Inc.. The 510(k) number is K932310.
When did KIT PAK INCONTINENT SKIN CARE KIT receive FDA 510(k) clearance?
KIT PAK INCONTINENT SKIN CARE KIT received FDA 510(k) clearance on 1994-06-01, under 510(k) number K932310.
Who is the listed applicant for KIT PAK INCONTINENT SKIN CARE KIT?
The FDA 510(k) record lists Kit Pak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KIT PAK INCONTINENT SKIN CARE KIT?
The FDA product code for KIT PAK INCONTINENT SKIN CARE KIT is EYQ.
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 Kit Pak, 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.
Related Devices (Code: EYQ)
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
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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