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FDA 510(k)

MID-STREAM COLLECTION SET-STERILE

K-Number: K953929 · 1995-11-16

ApplicantTrinity Laboratories, Inc.
Decision Date1995-11-16
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MID-STREAM COLLECTION SET-STERILE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1995-11-16 under 510(k) number K953929. 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 MID-STREAM COLLECTION SET-STERILE?

MID-STREAM COLLECTION SET-STERILE is a medical device that received FDA 510(k) clearance on 1995-11-16. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K953929.

When did MID-STREAM COLLECTION SET-STERILE receive FDA 510(k) clearance?

MID-STREAM COLLECTION SET-STERILE received FDA 510(k) clearance on 1995-11-16, under 510(k) number K953929.

Who is the listed applicant for MID-STREAM COLLECTION SET-STERILE?

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

What is the FDA product code for MID-STREAM COLLECTION SET-STERILE?

The FDA product code for MID-STREAM COLLECTION SET-STERILE is LIO.

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Other records listing Trinity Laboratories, 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.

K981441HEART CATH TRAY, STERILE, DISPOSABLEK974238DENTAL TRAY, STERILE, DISPOSABLEK974286CIRCUMCISION TRAY, CAT. NO. 70340K972160CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TESTK970722EYE TRAYK965201O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE

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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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