PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER
K-Number: K881057 · 1988-03-22
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Device Summary
Frequently Asked Questions
What is the PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER?
PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER is a medical device that received FDA 510(k) clearance on 1988-03-22. The listed applicant is Playtex, Inc.. The 510(k) number is K881057.
When did PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER receive FDA 510(k) clearance?
PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER received FDA 510(k) clearance on 1988-03-22, under 510(k) number K881057.
Who is the listed applicant for PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER?
The FDA 510(k) record lists Playtex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER?
The FDA product code for PLAYTEX PORTABLE NON-DEOD. & DEOD REGULAR & SUPER is HIL.
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 Playtex, 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: HIL)
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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