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FDA 510(k)

INSTRUMENT TIP PROTECTION COVERS

K-Number: K834127 · 1984-02-17

ApplicantDevon Industries, Inc.
Decision Date1984-02-17
Product CodeLXZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT TIP PROTECTION COVERS 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 1984-02-17 under 510(k) number K834127. The device is classified under product code LXZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT TIP PROTECTION COVERS?

INSTRUMENT TIP PROTECTION COVERS is a medical device that received FDA 510(k) clearance on 1984-02-17. The listed applicant is Devon Industries, Inc.. The 510(k) number is K834127.

When did INSTRUMENT TIP PROTECTION COVERS receive FDA 510(k) clearance?

INSTRUMENT TIP PROTECTION COVERS received FDA 510(k) clearance on 1984-02-17, under 510(k) number K834127.

Who is the listed applicant for INSTRUMENT TIP PROTECTION COVERS?

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 INSTRUMENT TIP PROTECTION COVERS?

The FDA product code for INSTRUMENT TIP PROTECTION COVERS is LXZ.

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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: LXZ)

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.

K955463GRIP-A-BOOTSSil-Med Corp.

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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