Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS

K-Number: K970968 · 1998-05-21

ApplicantGuenter Bissinger Medizintechnik GmbH
Decision Date1998-05-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Guenter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 1998-05-21 under 510(k) number K970968. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS?

BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS is a medical device that received FDA 510(k) clearance on 1998-05-21. The listed applicant is Guenter Bissinger Medizintechnik GmbH. The 510(k) number is K970968.

When did BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS receive FDA 510(k) clearance?

BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS received FDA 510(k) clearance on 1998-05-21, under 510(k) number K970968.

Who is the listed applicant for BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS?

The FDA 510(k) record lists Guenter Bissinger Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS?

The FDA product code for BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS is HET.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Guenter Bissinger Medizintechnik GmbH 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.

K213042Supra Non-Stick Bipolar ForcepsK051429CLARIS NON-STICK BIPOLAR FORCEPSK042077BITECH BIPOLAR SCISSORSK981919BISSINGER CABLES, CAT. NO. 801000XX

Related Devices (Code: HET)

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.

K250939SIRIUS Endoscope System (PR-SI-1230)Precision Robotics (Hong Kong) LimitedK243821i-CutA.M.I. Agency For Medical Innovations GmbHK221642SIRIUS Endoscope SystemPrecision Robotics (Hong Kong) LimitedK210116Video Endoscopy System, 3D Video Endoscopy SystemSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.K201832Endoeye Flex Deflectable Videoscope Olympus LTF-S190-5Olympus Medical Systems Corp.K210104SurroundScope System270surgical , Ltd.

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.

↑