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FDA 510(k)

Q-TIPS

K-Number: K770433 · 1977-04-15

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1977-04-15
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Q-TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770433. 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 Q-TIPS?

Q-TIPS is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K770433.

When did Q-TIPS receive FDA 510(k) clearance?

Q-TIPS received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770433.

Who is the listed applicant for Q-TIPS?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Q-TIPS?

The FDA product code for Q-TIPS is KXF.

Other records listing Chesebrough-Pond'S U.S.A. Co. 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.

K863866RESPIRADYNE II(TM)K862803CHESEBROUGH POND'S HYDROCOLLOID DRESSINGK851382CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSINGK851383BLISTERFILM TRANSPARENT DRESSINGK851539CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLOK843567KANGAROO NASOGASTRIC FEEDING TUBE

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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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