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FDA 510(k)

FORCEPS, PUNCHES, SCISSORS

K-Number: K943074 · 1994-08-02

Decision Date1994-08-02
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FORCEPS, PUNCHES, SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1994-08-02 under 510(k) number K943074. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, PUNCHES, SCISSORS?

FORCEPS, PUNCHES, SCISSORS is a medical device that received FDA 510(k) clearance on 1994-08-02. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K943074.

When did FORCEPS, PUNCHES, SCISSORS receive FDA 510(k) clearance?

FORCEPS, PUNCHES, SCISSORS received FDA 510(k) clearance on 1994-08-02, under 510(k) number K943074.

Who is the listed applicant for FORCEPS, PUNCHES, SCISSORS?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, PUNCHES, SCISSORS?

The FDA product code for FORCEPS, PUNCHES, SCISSORS is EOB.

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 KARL STORZ Endoscopy-America, 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.

View all 355 devices →

Related Devices (Code: EOB)

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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