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FDA 510(k)

HESSBURG-BFRRON TREPHINE

K-Number: K801585 · 1980-10-03

ApplicantPrecision Instruments, Inc.
Decision Date1980-10-03
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HESSBURG-BFRRON TREPHINE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Instruments, Inc.. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K801585. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HESSBURG-BFRRON TREPHINE?

HESSBURG-BFRRON TREPHINE is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Precision Instruments, Inc.. The 510(k) number is K801585.

When did HESSBURG-BFRRON TREPHINE receive FDA 510(k) clearance?

HESSBURG-BFRRON TREPHINE received FDA 510(k) clearance on 1980-10-03, under 510(k) number K801585.

Who is the listed applicant for HESSBURG-BFRRON TREPHINE?

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

What is the FDA product code for HESSBURG-BFRRON TREPHINE?

The FDA product code for HESSBURG-BFRRON TREPHINE is EMF.

Related Clinical Trials

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Other records listing Precision Instruments, Inc. 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.

K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONK860648BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIAK843048RING SUPPORTED TREPHINE FOR CORNEA TRANS

Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890217MICROSURGICAL KNIVESKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, Inc.

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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