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FDA 510(k)

DISPOSABLE SCISSORS

K-Number: K920297 · 1992-09-11

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

Device Summary

DISPOSABLE SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Falcon Instruments, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K920297. 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 DISPOSABLE SCISSORS?

DISPOSABLE SCISSORS is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Falcon Instruments, Inc.. The 510(k) number is K920297.

When did DISPOSABLE SCISSORS receive FDA 510(k) clearance?

DISPOSABLE SCISSORS received FDA 510(k) clearance on 1992-09-11, under 510(k) number K920297.

Who is the listed applicant for DISPOSABLE SCISSORS?

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

What is the FDA product code for DISPOSABLE SCISSORS?

The FDA product code for DISPOSABLE SCISSORS is MDM.

Related Clinical Trials

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Other records listing Falcon Instruments, 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.

K930775DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETCK920296DISPOSABLE FORCEPSK920298DISPOSABLE HEMOSTATS

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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