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FDA 510(k)

COTTON SWABS

K-Number: K820962 · 1982-04-20

ApplicantDafoe & Dafoe, Inc.
Decision Date1982-04-20
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COTTON SWABS is the device name listed in this FDA 510(k) record. The listed applicant is Dafoe & Dafoe, Inc.. It received FDA 510(k) clearance on 1982-04-20 under 510(k) number K820962. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COTTON SWABS?

COTTON SWABS is a medical device that received FDA 510(k) clearance on 1982-04-20. The listed applicant is Dafoe & Dafoe, Inc.. The 510(k) number is K820962.

When did COTTON SWABS receive FDA 510(k) clearance?

COTTON SWABS received FDA 510(k) clearance on 1982-04-20, under 510(k) number K820962.

Who is the listed applicant for COTTON SWABS?

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

What is the FDA product code for COTTON SWABS?

The FDA product code for COTTON SWABS is KXF.

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.

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Other records listing Dafoe & Dafoe, 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.

K820960MAXI & MINI SHIELDSK820961INCONTINENCE PAD OR ADULT DIAPERK800747BELTLESS MAXI, MINI & SUPER MAXI PADS

Related Devices (Code: KXF)

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.

K123184FINN CHAMBERS AQUASmartpracticeK103409ALLERGEAZE R CLEARSmartpracticeK063160ALLERGEAZE PATCH TEST CHAMBERSSmartpracticeK013820FINN CHAMBER (R)Epitest Ltd. OYK992553IQ CHAMBERSDormer Laboratories, Inc.K870762EAR APPLICATOR, CATALOG NO. 2229Treace Medical, Inc.

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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