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FDA 510(k)

MOUNTABLE KNIFE

K-Number: K931323 · 1994-04-28

ApplicantEsco Medical
Decision Date1994-04-28
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOUNTABLE KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Esco Medical. It received FDA 510(k) clearance on 1994-04-28 under 510(k) number K931323. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOUNTABLE KNIFE?

MOUNTABLE KNIFE is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Esco Medical. The 510(k) number is K931323.

When did MOUNTABLE KNIFE receive FDA 510(k) clearance?

MOUNTABLE KNIFE received FDA 510(k) clearance on 1994-04-28, under 510(k) number K931323.

Who is the listed applicant for MOUNTABLE KNIFE?

The FDA 510(k) record lists Esco Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOUNTABLE KNIFE?

The FDA product code for MOUNTABLE KNIFE is HRX.

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.

Related Devices (Code: HRX)

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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