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FDA 510(k)

DISPOSABLE FORCEPS

K-Number: K920296 · 1992-09-11

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

Device Summary

DISPOSABLE FORCEPS 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 K920296. 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 FORCEPS?

DISPOSABLE FORCEPS 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 K920296.

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

DISPOSABLE FORCEPS received FDA 510(k) clearance on 1992-09-11, under 510(k) number K920296.

Who is the listed applicant for DISPOSABLE FORCEPS?

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 FORCEPS?

The FDA product code for DISPOSABLE FORCEPS is MDM.

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.

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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, ETCK920297DISPOSABLE SCISSORSK920298DISPOSABLE 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

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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