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FDA 510(k)

CIT BIOPSY PUNCHES

K-Number: K944444 · 1995-09-29

ApplicantChirurgische Instrumente
Decision Date1995-09-29
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CIT BIOPSY PUNCHES is the device name listed in this FDA 510(k) record. The listed applicant is Chirurgische Instrumente. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K944444. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIT BIOPSY PUNCHES?

CIT BIOPSY PUNCHES is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Chirurgische Instrumente. The 510(k) number is K944444.

When did CIT BIOPSY PUNCHES receive FDA 510(k) clearance?

CIT BIOPSY PUNCHES received FDA 510(k) clearance on 1995-09-29, under 510(k) number K944444.

Who is the listed applicant for CIT BIOPSY PUNCHES?

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

What is the FDA product code for CIT BIOPSY PUNCHES?

The FDA product code for CIT BIOPSY PUNCHES is HFB.

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.

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Other records listing Chirurgische Instrumente 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.

K944270CIT MONOPOLAR LAPAROSCOPIC INSTRMENTSK944268CIT TWO WAY SUCTIN AND IRRIGATION TUBESK944269CIT GRASPING AND DISSECTING FORCEPS

Related Devices (Code: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.K926538TISCHLER BIOPSY FORCEPSThomasville Medical Assoc.

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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