FDA 510(k)

GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH

K-Number: K953868 · 1995-09-29

ApplicantRichard Wolf Medical Instruments Corp.

Decision Date1995-09-29

Product CodeHRX

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K953868. 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 GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH?

GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K953868.

When did GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH receive FDA 510(k) clearance?

GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH received FDA 510(k) clearance on 1995-09-29, under 510(k) number K953868.

Who is the listed applicant for GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH?

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

What is the FDA product code for GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH?

The FDA product code for GRASPING FORCEPS, BIOPSY FORCEPS, SCISSORS, PUNCH is HRX.

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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.