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FDA 510(k)

STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE

K-Number: K923098 · 1992-09-21

ApplicantTrinity Laboratories, Inc.
Decision Date1992-09-21
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE 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 1992-09-21 under 510(k) number K923098. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE?

STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1992-09-21. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K923098.

When did STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE receive FDA 510(k) clearance?

STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE received FDA 510(k) clearance on 1992-09-21, under 510(k) number K923098.

Who is the listed applicant for STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE?

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 STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE?

The FDA product code for STERILE MUCOUS SPECIMEN TRAP, DISPOSABLE is BSY.

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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: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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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