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FDA 510(k)

PUNCH SURGICAL

K-Number: K933772 · 1994-02-01

ApplicantMahe-Medizintechnik
Decision Date1994-02-01
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PUNCH SURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Mahe-Medizintechnik. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K933772. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PUNCH SURGICAL?

PUNCH SURGICAL is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Mahe-Medizintechnik. The 510(k) number is K933772.

When did PUNCH SURGICAL receive FDA 510(k) clearance?

PUNCH SURGICAL received FDA 510(k) clearance on 1994-02-01, under 510(k) number K933772.

Who is the listed applicant for PUNCH SURGICAL?

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 PUNCH SURGICAL?

The FDA product code for PUNCH SURGICAL is LXH.

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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/BIOPSYK933770FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPEK935442MAHE INSTRUMENTS

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Related Devices (Code: LXH)

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.

K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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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