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FDA 510(k)

PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598

K-Number: K981760 · 1998-07-22

Decision Date1998-07-22
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598 is the device name listed in this FDA 510(k) record. The listed applicant is Playtime Products, Inc.. It received FDA 510(k) clearance on 1998-07-22 under 510(k) number K981760. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598?

PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598 is a medical device that received FDA 510(k) clearance on 1998-07-22. The listed applicant is Playtime Products, Inc.. The 510(k) number is K981760.

When did PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598 receive FDA 510(k) clearance?

PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598 received FDA 510(k) clearance on 1998-07-22, under 510(k) number K981760.

Who is the listed applicant for PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598?

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

What is the FDA product code for PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598?

The FDA product code for PLAYTEX SILK GLIDE ODOR ABSORBING FLUSHABLE CARDBOARD TAMPONS #13598 is HEB.

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 Playtime Products, 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 8 devices →

Related Devices (Code: HEB)

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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