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FDA 510(k)

DEVON HEAD REST

K-Number: K840422 · 1984-03-12

ApplicantDevon Industries, Inc.
Decision Date1984-03-12
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEVON HEAD REST 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 1984-03-12 under 510(k) number K840422. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVON HEAD REST?

DEVON HEAD REST is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Devon Industries, Inc.. The 510(k) number is K840422.

When did DEVON HEAD REST receive FDA 510(k) clearance?

DEVON HEAD REST received FDA 510(k) clearance on 1984-03-12, under 510(k) number K840422.

Who is the listed applicant for DEVON HEAD REST?

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 DEVON HEAD REST?

The FDA product code for DEVON HEAD REST is FWZ.

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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 DEVICEK943892POINT OF USE SHARPS A GATORK944114PHLEBOTOMY UNIT SHARPS A GATORK945197THE SHARPS COLLECTION AND DISPOSAL SYSTEM

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Related Devices (Code: FWZ)

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.

K960019RETRACTOR ARM CLAMPBiopsys Medical, Inc.K945415'LIL MAC ACCESSORY CLAMP(TM)D.L. Nelson and Assoc., Inc.K944779CARBON LIGHTS HAND SURGERY TABLEAllen Medical Systems, Inc.K935381KAPS POSITIONING ARMAndronic Devices, Ltd.K931037WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)Whitmore Ent., Inc.K926225SPONGE COUNTERAmerican Medical Manufacturer, 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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