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FDA 510(k)

DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE

K-Number: K922874 · 1992-09-11

ApplicantSupra Instruments, Inc.
Decision Date1992-09-11
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Supra Instruments, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K922874. 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 DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE?

DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Supra Instruments, Inc.. The 510(k) number is K922874.

When did DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE receive FDA 510(k) clearance?

DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE received FDA 510(k) clearance on 1992-09-11, under 510(k) number K922874.

Who is the listed applicant for DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE?

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

What is the FDA product code for DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE?

The FDA product code for DISPSABLE FORCEPS, HEMOSTATS, PROBES, NEEDLE GUIDE is MDM.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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