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FDA 510(k)

SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES

K-Number: K934332 · 1994-03-25

ApplicantFriatec Medical Inc., USA
Decision Date1994-03-25
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES is the device name listed in this FDA 510(k) record. The listed applicant is Friatec Medical Inc., USA. It received FDA 510(k) clearance on 1994-03-25 under 510(k) number K934332. 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 SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES?

SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES is a medical device that received FDA 510(k) clearance on 1994-03-25. The listed applicant is Friatec Medical Inc., USA. The 510(k) number is K934332.

When did SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES receive FDA 510(k) clearance?

SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES received FDA 510(k) clearance on 1994-03-25, under 510(k) number K934332.

Who is the listed applicant for SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES?

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

What is the FDA product code for SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES?

The FDA product code for SURGICAL INSTRUMENTS, FORCEPS & GRASPERS, PROBES & CURETTES is HRX.

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Other records listing Friatec Medical Inc., USA as applicant

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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.

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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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