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)

#820/821 BIPOLAR FORCEPS

K-Number: K884175 · 1988-10-24

ApplicantOlsen Electrosurgical, Inc.
Decision Date1988-10-24
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

#820/821 BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Olsen Electrosurgical, Inc.. It received FDA 510(k) clearance on 1988-10-24 under 510(k) number K884175. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the #820/821 BIPOLAR FORCEPS?

#820/821 BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1988-10-24. The listed applicant is Olsen Electrosurgical, Inc.. The 510(k) number is K884175.

When did #820/821 BIPOLAR FORCEPS receive FDA 510(k) clearance?

#820/821 BIPOLAR FORCEPS received FDA 510(k) clearance on 1988-10-24, under 510(k) number K884175.

Who is the listed applicant for #820/821 BIPOLAR FORCEPS?

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

What is the FDA product code for #820/821 BIPOLAR FORCEPS?

The FDA product code for #820/821 BIPOLAR FORCEPS is HAM.

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 Olsen Electrosurgical, 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.

K922154INSULATED SPECULUM W/ SMOKE EVACUATOR OPTIONK912611OLSEN LAPAROSCOPIC INSTR, DISPOSABLE, SINGLE USEK913108TEFLON COATED ELECTRODES/ELECTRODES HANDLESK912612SMOKE/ODOR EVACUATOR #757K885199#500 SERIES FORCEPS W/CUT/COAGULATE SWITCHESK885200600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE

View all 11 devices →

Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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.

↑