PLAYTEX COMBINATION FIBER MODIFIED TAMP
K-Number: K811387 · 1981-08-07
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Device Summary
Frequently Asked Questions
What is the PLAYTEX COMBINATION FIBER MODIFIED TAMP?
PLAYTEX COMBINATION FIBER MODIFIED TAMP is a medical device that received FDA 510(k) clearance on 1981-08-07. The listed applicant is Playtex, Inc.. The 510(k) number is K811387.
When did PLAYTEX COMBINATION FIBER MODIFIED TAMP receive FDA 510(k) clearance?
PLAYTEX COMBINATION FIBER MODIFIED TAMP received FDA 510(k) clearance on 1981-08-07, under 510(k) number K811387.
Who is the listed applicant for PLAYTEX COMBINATION FIBER MODIFIED TAMP?
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 COMBINATION FIBER MODIFIED TAMP?
The FDA product code for PLAYTEX COMBINATION FIBER MODIFIED TAMP 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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