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FDA 510(k)

MODIFIED OLSEN 755/756 SWITCHPENS

K-Number: K884174 · 1988-10-24

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

Device Summary

MODIFIED OLSEN 755/756 SWITCHPENS 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 K884174. 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 MODIFIED OLSEN 755/756 SWITCHPENS?

MODIFIED OLSEN 755/756 SWITCHPENS 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 K884174.

When did MODIFIED OLSEN 755/756 SWITCHPENS receive FDA 510(k) clearance?

MODIFIED OLSEN 755/756 SWITCHPENS received FDA 510(k) clearance on 1988-10-24, under 510(k) number K884174.

Who is the listed applicant for MODIFIED OLSEN 755/756 SWITCHPENS?

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 MODIFIED OLSEN 755/756 SWITCHPENS?

The FDA product code for MODIFIED OLSEN 755/756 SWITCHPENS is HAM.

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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

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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.

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