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FDA 510(k)

EASY-ON

K-Number: K932998 · 1993-08-18

ApplicantDevon Industries, Inc.
Decision Date1993-08-18
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EASY-ON is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1993-08-18 under 510(k) number K932998. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY-ON?

EASY-ON is a medical device that received FDA 510(k) clearance on 1993-08-18. The listed applicant is Devon Industries, Inc.. The 510(k) number is K932998.

When did EASY-ON receive FDA 510(k) clearance?

EASY-ON received FDA 510(k) clearance on 1993-08-18, under 510(k) number K932998.

Who is the listed applicant for EASY-ON?

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

What is the FDA product code for EASY-ON?

The FDA product code for EASY-ON is GES.

Other records listing Devon Industries, 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.

K961993BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)K954015ABG POINT LOK NEEDLE PROTECTION DEVICEK946289DEVONS POINT LOK NEEDLE PROTECTION DEVICEK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEMK944114PHLEBOTOMY UNIT SHARPS A GATORK943892POINT OF USE SHARPS A GATOR

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Related Devices (Code: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK900266STERILE CARBON STEEL SURGICAL BLADERahn LaboratoriesK884862ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADEAnchor Products Co.

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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