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FDA 510(k)

ACCU-CULT FECAL OCCULT BLOOD TEST

K-Number: K840904 · 1984-08-16

ApplicantApplied Medical Devices, Inc.
Decision Date1984-08-16
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ACCU-CULT FECAL OCCULT BLOOD TEST is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Devices, Inc.. It received FDA 510(k) clearance on 1984-08-16 under 510(k) number K840904. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-CULT FECAL OCCULT BLOOD TEST?

ACCU-CULT FECAL OCCULT BLOOD TEST is a medical device that received FDA 510(k) clearance on 1984-08-16. The listed applicant is Applied Medical Devices, Inc.. The 510(k) number is K840904.

When did ACCU-CULT FECAL OCCULT BLOOD TEST receive FDA 510(k) clearance?

ACCU-CULT FECAL OCCULT BLOOD TEST received FDA 510(k) clearance on 1984-08-16, under 510(k) number K840904.

Who is the listed applicant for ACCU-CULT FECAL OCCULT BLOOD TEST?

The FDA 510(k) record lists Applied Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCU-CULT FECAL OCCULT BLOOD TEST?

The FDA product code for ACCU-CULT FECAL OCCULT BLOOD TEST is KHE.

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Other records listing Applied Medical Devices, Inc. as applicant

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K843885PERCUTANEOUS ASPIRATION BIOPSY TRAYK843883STERILE PERCUTANEOUS TRANSHEPATIC CHOLANK843884GENERAL UTILITY TRAY SYSTEMK842591ULTRASOUND PROBE COVERS-STERILEK833720TRANSTHORACIC/TRANSABDOMINAL-TRAYK840334CHEMONUCLEOLYSIS/DISCOGRAPHY TRAY

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Related Devices (Code: KHE)

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.

K173212Instant-view-PLUS immunochemical Fecal Occult Blood TestAlfa Scientific Designs, Inc.K170548InSure ONEEnterix, Inc.K171484hema-screen SPECIFIC GoldImmunostics Inc.,K162333Wondfo One Step Fecal Occult Blood (FOB) TestGuangzhou Wondfo Biotech Co., Ltd.K163554hema-screen ER XCEL Enhanced Readability Fecal Occult Blood TestImmunostics Inc.,K121397OSOM IFOB 25 TEST AND PATIENT COLLECTION KIT OSOM IFOB CONTROL KIT OSOM IFOB 50 TEST KITSEKISUI Diagnostics, LLC

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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