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FDA 510(k)

CHANGING METHOD OF STERILITY RELEASE

K-Number: K832368 · 1983-10-31

ApplicantDevon Industries, Inc.
Decision Date1983-10-31
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHANGING METHOD OF STERILITY RELEASE 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 1983-10-31 under 510(k) number K832368. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHANGING METHOD OF STERILITY RELEASE?

CHANGING METHOD OF STERILITY RELEASE is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Devon Industries, Inc.. The 510(k) number is K832368.

When did CHANGING METHOD OF STERILITY RELEASE receive FDA 510(k) clearance?

CHANGING METHOD OF STERILITY RELEASE received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832368.

Who is the listed applicant for CHANGING METHOD OF STERILITY RELEASE?

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 CHANGING METHOD OF STERILITY RELEASE?

The FDA product code for CHANGING METHOD OF STERILITY RELEASE is EMF.

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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: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890217MICROSURGICAL KNIVESKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, 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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