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FDA 510(k)

DUPONT ISOLATOR 1.5 MICROBIAL TUBE

K-Number: K832246 · 1983-09-26

ApplicantE.I. Dupont DE Nemours & Co., Inc.
Decision Date1983-09-26
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DUPONT ISOLATOR 1.5 MICROBIAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832246. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUPONT ISOLATOR 1.5 MICROBIAL TUBE?

DUPONT ISOLATOR 1.5 MICROBIAL TUBE is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K832246.

When did DUPONT ISOLATOR 1.5 MICROBIAL TUBE receive FDA 510(k) clearance?

DUPONT ISOLATOR 1.5 MICROBIAL TUBE received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832246.

Who is the listed applicant for DUPONT ISOLATOR 1.5 MICROBIAL TUBE?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUPONT ISOLATOR 1.5 MICROBIAL TUBE?

The FDA product code for DUPONT ISOLATOR 1.5 MICROBIAL TUBE is LIO.

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Other records listing E.I. Dupont DE Nemours & Co., Inc. as applicant

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Related Devices (Code: LIO)

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.

K222613ARX Liquid Amies Collection & Transport SystemArx Sciences, Inc.K131630PURITAN AMIES MEDIUM COLLECTION AND TRANSPORT SYSTEMPuritan Medical Products, LLCK120846TRANSPORT CULTURE MEDIUM DEVICEPuritan Medical Products, LLCK103805MEDICAL WIRE & EQUIPMENT S-TRANSWAB (OR SIGMA-TRANSWAB) LIQUID AMIES COLLECTION AND TRANSPORT DEVICEMedical Wire & Equipment Company (Bath), Ltd.K082472VIROCULT, MODEL MW950Medical Wire & Equipment Company (Bath), Ltd.K070062COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USEDiesse Diagnostica Senese S.P.A.

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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