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FDA 510(k)

PAD HOLDER KIT

K-Number: K780867 · 1978-08-14

ApplicantDevon Industries, Inc.
Decision Date1978-08-14
Product CodeFSE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PAD HOLDER KIT 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 1978-08-14 under 510(k) number K780867. The device is classified under product code FSE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAD HOLDER KIT?

PAD HOLDER KIT is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Devon Industries, Inc.. The 510(k) number is K780867.

When did PAD HOLDER KIT receive FDA 510(k) clearance?

PAD HOLDER KIT received FDA 510(k) clearance on 1978-08-14, under 510(k) number K780867.

Who is the listed applicant for PAD HOLDER KIT?

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 PAD HOLDER KIT?

The FDA product code for PAD HOLDER KIT is FSE.

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Other records listing Devon Industries, Inc. as applicant

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K961993BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)K954015ABG POINT LOK NEEDLE PROTECTION DEVICEK946289DEVONS POINT LOK NEEDLE PROTECTION DEVICEK944114PHLEBOTOMY UNIT SHARPS A GATORK943892POINT OF USE SHARPS A GATORK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEM

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Related Devices (Code: FSE)

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.

K860503THE POREX RETRACTOR TABLEPorex MedicalK843801MASON EQUIPMENT ORGANIZER & ASPENAspen Laboratories, Inc.K840027OPERATING ROOM STANDHealthmate, Inc.K831042CHEMONUCLEOLYSIS TABLE EXTENSIONOrthopedic Systems, Inc.K830339IMSI/METRIPOND HAND OPERATING TABLEIntl. Management Services, Inc.K822427SELF-CONTAINED MOBILE OPHTHAL. OPER. .Surgi-Quip Inc.U

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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