Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SURGICAL INSTRUMENT KIT, DISPOSABLE

K-Number: K920989 · 1992-10-19

ApplicantUlti-Med Intl., Inc.
Decision Date1992-10-19
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

SURGICAL INSTRUMENT KIT, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 1992-10-19 under 510(k) number K920989. 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 SURGICAL INSTRUMENT KIT, DISPOSABLE?

SURGICAL INSTRUMENT KIT, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1992-10-19. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K920989.

When did SURGICAL INSTRUMENT KIT, DISPOSABLE receive FDA 510(k) clearance?

SURGICAL INSTRUMENT KIT, DISPOSABLE received FDA 510(k) clearance on 1992-10-19, under 510(k) number K920989.

Who is the listed applicant for SURGICAL INSTRUMENT KIT, DISPOSABLE?

The FDA 510(k) record lists Ulti-Med Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL INSTRUMENT KIT, DISPOSABLE?

The FDA product code for SURGICAL INSTRUMENT KIT, DISPOSABLE is KDD.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ulti-Med Intl., 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.

K103011ULTICARE SAFETY INSULIN SYRINGEK923176SURGICAL INSTRUMENT KIT, DISPOSABLEK923175SURGICAL INSTRUMENT KIT, DISPOSABLEK922828ULCER WOUND TRAYK914244STERILE CUSTOM SURGICAL KITSK914431ABSORBENT FIBER

View all 21 devices →

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.

↑