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FDA 510(k)

DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)

K-Number: K902441 · 1990-08-23

ApplicantCurrie Medical Specialties, Inc.
Decision Date1990-08-23
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS) is the device name listed in this FDA 510(k) record. The listed applicant is Currie Medical Specialties, Inc.. It received FDA 510(k) clearance on 1990-08-23 under 510(k) number K902441. 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 DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)?

DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS) is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K902441.

When did DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS) receive FDA 510(k) clearance?

DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS) received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902441.

Who is the listed applicant for DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)?

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

What is the FDA product code for DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS)?

The FDA product code for DISPOSABLE PROCEDURAL TRAYS #CK-XXXXX (VARIOUS) is KDD.

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Related Devices (Code: KDD)

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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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