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FDA 510(k)

CENTURION DISPOSABLE INSTRUMENTS

K-Number: K923812 · 1992-12-17

ApplicantTri-State Hospital Supply Corp.
Decision Date1992-12-17
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CENTURION DISPOSABLE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Tri-State Hospital Supply Corp.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K923812. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTURION DISPOSABLE INSTRUMENTS?

CENTURION DISPOSABLE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Tri-State Hospital Supply Corp.. The 510(k) number is K923812.

When did CENTURION DISPOSABLE INSTRUMENTS receive FDA 510(k) clearance?

CENTURION DISPOSABLE INSTRUMENTS received FDA 510(k) clearance on 1992-12-17, under 510(k) number K923812.

Who is the listed applicant for CENTURION DISPOSABLE INSTRUMENTS?

The FDA 510(k) record lists Tri-State Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTURION DISPOSABLE INSTRUMENTS?

The FDA product code for CENTURION DISPOSABLE INSTRUMENTS is MDM.

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Other records listing Tri-State Hospital Supply Corp. 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.

K080448CENTURION PROTECTIVE RESTRAINT, SCR SERIESK080524CENTURION SORBAVIEW OTCK942353CENTURION UMBILICAL CATHETERK945977CENTURION(R) SITE GUARD(R) TRANSPARENT DRESSING/TRANSPAENT FILM DRESSINGK931748CENTLURION DISP STERI DENTAL/HYGIENE PACK/TRAYSK935491CENTURION MOGEN CLAMP/CIRCUMCISION (STER/NON STER)

View all 16 devices →

Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, 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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