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FDA 510(k)

DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC

K-Number: K930775 · 1993-04-23

Decision Date1993-04-23
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC 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 1993-04-23 under 510(k) number K930775. 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, HEMOSTATS, NEEDLE GUIDES, ETC?

DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Falcon Instruments, Inc.. The 510(k) number is K930775.

When did DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC receive FDA 510(k) clearance?

DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC received FDA 510(k) clearance on 1993-04-23, under 510(k) number K930775.

Who is the listed applicant for DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC?

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, HEMOSTATS, NEEDLE GUIDES, ETC?

The FDA product code for DISPOSABLE FORCEPS, HEMOSTATS, NEEDLE GUIDES, ETC 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.

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.

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.

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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