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FDA 510(k)

GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB

K-Number: K920516 · 1992-04-16

ApplicantTrinity Laboratories, Inc.
Decision Date1992-04-16
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB 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 1992-04-16 under 510(k) number K920516. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB?

GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB is a medical device that received FDA 510(k) clearance on 1992-04-16. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K920516.

When did GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB receive FDA 510(k) clearance?

GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB received FDA 510(k) clearance on 1992-04-16, under 510(k) number K920516.

Who is the listed applicant for GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB?

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 GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB?

The FDA product code for GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB is KDD.

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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: KDD)

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.

K072814CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURESCovidienK011514INSTRUMENTS FOR ONE TIME USE - DISPOSABLEKencap , Ltd.K971317NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYSNational Healthcare Mfg. Corp.K960456DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAYDenver Biomaterials, Inc.K936255CUSTOM CV PACKAssociated MedicalK932219SUTURE SET OR LACERATION TRAYS (PACKS)Associated Medical Products Co.

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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