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FDA 510(k)

STOOL TRANSPORT/PROCESSOR

K-Number: K933370 · 1994-02-17

ApplicantSage Products, Inc.
Decision Date1994-02-17
Product CodeLKS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

STOOL TRANSPORT/PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1994-02-17 under 510(k) number K933370. The device is classified under product code LKS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOOL TRANSPORT/PROCESSOR?

STOOL TRANSPORT/PROCESSOR is a medical device that received FDA 510(k) clearance on 1994-02-17. The listed applicant is Sage Products, Inc.. The 510(k) number is K933370.

When did STOOL TRANSPORT/PROCESSOR receive FDA 510(k) clearance?

STOOL TRANSPORT/PROCESSOR received FDA 510(k) clearance on 1994-02-17, under 510(k) number K933370.

Who is the listed applicant for STOOL TRANSPORT/PROCESSOR?

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

What is the FDA product code for STOOL TRANSPORT/PROCESSOR?

The FDA product code for STOOL TRANSPORT/PROCESSOR is LKS.

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Other records listing Sage Products, 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.

K972705RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTICK980490SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPSK9739112 GALLON ALTERNATE CARE SHARPS CONTAINERK972279SHARPS SHUTTLEK970135NITRILE GLOVESK972302POCKET COUNT OR SAFETCOUNT

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Related Devices (Code: LKS)

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.

K053257PARA-PRO FC50Alpha-Tec Systems, Inc.K021420PARACON II/FECAL CONCENTRATOR IIPara Scientific Co.K980077PARA-PAK SPINCONMeridian Diagnostics, Inc.K941110PARAKITHardy DiagnosticsK941129CON-KITMedical Chemical Corp.K935316PARASAFE(R) FIXATIVEScientific Device Laboratory, 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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