Conphar Exam. Gloves, Polyethylene

FDA 510(k) K791805 · Conphar, Inc.

Substantially Equivalent

510(k) numberK791805

Submission

Device name
Conphar Exam. Gloves, Polyethylene
Applicant
Conphar, Inc.
Mchenry, IL, US
Received
September 13, 1979
Decision date
October 1, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FMC – Patient Examination Glove
Device class
Class I (low risk)
Regulation
21 CFR 880.6250
Specialty
General Hospital

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K014134Powder-Free Latex Exam Gloves with Protein Labeling (<50UG/G)FMC · Traditional Supergrade Healthcare Products Sdn. Bhd.01/22/2002SE
K992337Blossom Powder Free Latex Examination Gloves with Protein Content Labeling Claim 50 MCGM…FMC · Traditional Mexpo Intl., Inc.08/17/1999SE
K932405Nitrile Rubber Examination Gloves (Powered)FMC · Traditional Safeskin Corp.05/18/1994SE
K932404Nitrile Rubber Powder-Free Examination GloveFMC · Traditional Safeskin Corp.05/18/1994SE
K923175Surgical Instrument Kit, DisposableFMC · Traditional Ulti-Med Intl., Inc.06/17/1993SE
K920649CompasepFMC · Traditional Wilde-USA, Inc.07/23/1992SE
K915376Glasion VarnishFMC · Traditional Sci-Pharm Scientific Pharmaceutical, Inc.01/22/1992SE
K905127Latex Glove Application and Removal SystemFMC · Traditional Success Builders Intl., Inc.01/30/1991SE
K905109Patient Examination Glove/HypoallergenicFMC · Traditional Tactyl Technologies, Inc.11/21/1990SE

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Questions and answers

When was Conphar Exam. Gloves, Polyethylene cleared by the FDA?

Conphar Exam. Gloves, Polyethylene (K791805) received a 510(k) decision of Substantially Equivalent on October 1, 1979, 18 days after the submission was received.

What is the product code of K791805?

The FDA product code is FMC – Patient Examination Glove, a Class I (low risk) device regulated under 21 CFR 880.6250.