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FDA 510(k)

ENDOCOAGULATOR 2001 KLI

K-Number: K895402 · 1990-04-26

ApplicantCabot Medical Corp.
Decision Date1990-04-26
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENDOCOAGULATOR 2001 KLI is the device name listed in this FDA 510(k) record. The listed applicant is Cabot Medical Corp.. It received FDA 510(k) clearance on 1990-04-26 under 510(k) number K895402. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOCOAGULATOR 2001 KLI?

ENDOCOAGULATOR 2001 KLI is a medical device that received FDA 510(k) clearance on 1990-04-26. The listed applicant is Cabot Medical Corp.. The 510(k) number is K895402.

When did ENDOCOAGULATOR 2001 KLI receive FDA 510(k) clearance?

ENDOCOAGULATOR 2001 KLI received FDA 510(k) clearance on 1990-04-26, under 510(k) number K895402.

Who is the listed applicant for ENDOCOAGULATOR 2001 KLI?

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

What is the FDA product code for ENDOCOAGULATOR 2001 KLI?

The FDA product code for ENDOCOAGULATOR 2001 KLI is HGI.

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Other records listing Cabot Medical Corp. 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.

K960148CIRCON-SURGITEK CLASSIC DOUBLE PIGTAIL URETERAL STENTK946109CABOT MEDICAL REUSABLE BIPOLAR CUTTING FORCEPSK951972CABOT MEDICAL ULTRA FLOW CYSTOURETHROSCOPE SYSTEM WITH OPERATING & DIAGNOSTIC SHEATHSK951714CABOT MEDICAL-SURGITEK ULTRAGOLD PLUS SIDE-FIRING UROLOGIC LASER FIBERK941743CABOT MEDICAL NIAGARA FLUID MANAGEMENT PUMPK9341153000 ELECTRONIC INSUFFLATOR MODIFICATION

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Related Devices (Code: HGI)

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.

K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLCK152843Liger Medical HTU-110Liger Medical, LLCK121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, 155, 157 AND 158Apple Medical Corp.K022593THOMAS MEDICAL ELECTRODESThomas Medical, 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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