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FDA 510(k)

FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE

K-Number: K933770 · 1994-03-23

ApplicantMahe-Medizintechnik
Decision Date1994-03-23
Product CodeLRC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE is the device name listed in this FDA 510(k) record. The listed applicant is Mahe-Medizintechnik. It received FDA 510(k) clearance on 1994-03-23 under 510(k) number K933770. The device is classified under product code LRC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE?

FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE is a medical device that received FDA 510(k) clearance on 1994-03-23. The listed applicant is Mahe-Medizintechnik. The 510(k) number is K933770.

When did FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE receive FDA 510(k) clearance?

FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE received FDA 510(k) clearance on 1994-03-23, under 510(k) number K933770.

Who is the listed applicant for FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE?

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

What is the FDA product code for FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE?

The FDA product code for FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE is LRC.

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Other records listing Mahe-Medizintechnik 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.

K942821MAHE INSTRUMENTSK942819TROCAR WITH SHIELDK933768COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIESK933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYK935442MAHE INSTRUMENTSK933772PUNCH SURGICAL

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Related Devices (Code: LRC)

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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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