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FDA 510(k)

TITANIUM CONNECTOR (2 PART)

K-Number: K910787 · 1991-08-15

ApplicantAccurate Surgical Instruments Co.
Decision Date1991-08-15
Product CodeFKO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TITANIUM CONNECTOR (2 PART) is the device name listed in this FDA 510(k) record. The listed applicant is Accurate Surgical Instruments Co.. It received FDA 510(k) clearance on 1991-08-15 under 510(k) number K910787. The device is classified under product code FKO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM CONNECTOR (2 PART)?

TITANIUM CONNECTOR (2 PART) is a medical device that received FDA 510(k) clearance on 1991-08-15. The listed applicant is Accurate Surgical Instruments Co.. The 510(k) number is K910787.

When did TITANIUM CONNECTOR (2 PART) receive FDA 510(k) clearance?

TITANIUM CONNECTOR (2 PART) received FDA 510(k) clearance on 1991-08-15, under 510(k) number K910787.

Who is the listed applicant for TITANIUM CONNECTOR (2 PART)?

The FDA 510(k) record lists Accurate Surgical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM CONNECTOR (2 PART)?

The FDA product code for TITANIUM CONNECTOR (2 PART) is FKO.

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Other records listing Accurate Surgical Instruments Co. 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.

K950042SWAN NECK PRESTERNAL PERITONEAL DIALYSIS CATHETERK920515INSERTIONK910786TROCAR (FALLER STYLET)K910785TITANIUM CATHETER EXTENDERK862046SWAN-NECK PERITONEAL DIALYSIS CATHETERSK850214STERILE CATHETERS-CATHETER PERITONEAL LONG-TERM IN

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Related Devices (Code: FKO)

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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISCorpak, Inc.K974570PERITONEAL DIALYSIS CATHETER CONNECTORMedigroup, Inc.K885037AMUKIN 50% - AIRSPRAY(R)Bernard J. Cooney, P.A.K874650PERITONEAL DIALYSIS KIT (ACUTE AND CHRONIC FORM)Quinton, Inc.K872221DIALY-NATE SET & DIALY-NATE CATHETERGesco Intl., Inc.K871730MODIFIED USE OF PULL-APART INTRODUCER SETQuinton, 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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