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FDA 510(k)

STERILE RUBBER BANDS

K-Number: K834063 · 1983-12-22

ApplicantDevon Industries, Inc.
Decision Date1983-12-22
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE RUBBER BANDS 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 1983-12-22 under 510(k) number K834063. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE RUBBER BANDS?

STERILE RUBBER BANDS is a medical device that received FDA 510(k) clearance on 1983-12-22. The listed applicant is Devon Industries, Inc.. The 510(k) number is K834063.

When did STERILE RUBBER BANDS receive FDA 510(k) clearance?

STERILE RUBBER BANDS received FDA 510(k) clearance on 1983-12-22, under 510(k) number K834063.

Who is the listed applicant for STERILE RUBBER BANDS?

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 STERILE RUBBER BANDS?

The FDA product code for STERILE RUBBER BANDS is LDQ.

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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: LDQ)

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K993797EC-7701 FLUID WARMING CABINETEnthermics Medical Systems, Inc.K992258HOT SHOT FLUID WARMER IV FLUIDSInfra-Med Technologies, Inc.K981032PIV SYSTEMMedical Solutions, Inc.K973747CONTROLLED TEMPERATURE CABINET SYSTEMSmithK955661ACU-HALTGlederer & Co., Inc.K955776ACU-LABGlederer & Co., 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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