Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HAND-HELD HEAT APPLICATOR

K-Number: K935995 · 1994-06-09

Decision Date1994-06-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

HAND-HELD HEAT APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Avon Products, Inc.. It received FDA 510(k) clearance on 1994-06-09 under 510(k) number K935995. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HAND-HELD HEAT APPLICATOR?

HAND-HELD HEAT APPLICATOR is a medical device that received FDA 510(k) clearance on 1994-06-09. The listed applicant is Avon Products, Inc.. The 510(k) number is K935995.

When did HAND-HELD HEAT APPLICATOR receive FDA 510(k) clearance?

HAND-HELD HEAT APPLICATOR received FDA 510(k) clearance on 1994-06-09, under 510(k) number K935995.

Who is the listed applicant for HAND-HELD HEAT APPLICATOR?

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

What is the FDA product code for HAND-HELD HEAT APPLICATOR?

The FDA product code for HAND-HELD HEAT APPLICATOR is ILY.

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 Avon 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.

Related Devices (Code: ILY)

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.

↑