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FDA 510(k)

CABOT LASER LAPAROSCOPY ACCESSORY SET

K-Number: K862228 · 1986-08-20

ApplicantCabot Medical Corp.
Decision Date1986-08-20
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CABOT LASER LAPAROSCOPY ACCESSORY SET 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 1986-08-20 under 510(k) number K862228. The device is classified under product code HHR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CABOT LASER LAPAROSCOPY ACCESSORY SET?

CABOT LASER LAPAROSCOPY ACCESSORY SET is a medical device that received FDA 510(k) clearance on 1986-08-20. The listed applicant is Cabot Medical Corp.. The 510(k) number is K862228.

When did CABOT LASER LAPAROSCOPY ACCESSORY SET receive FDA 510(k) clearance?

CABOT LASER LAPAROSCOPY ACCESSORY SET received FDA 510(k) clearance on 1986-08-20, under 510(k) number K862228.

Who is the listed applicant for CABOT LASER LAPAROSCOPY ACCESSORY SET?

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 CABOT LASER LAPAROSCOPY ACCESSORY SET?

The FDA product code for CABOT LASER LAPAROSCOPY ACCESSORY SET is HHR.

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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: HHR)

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.

K881507ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIESHgm Medical Laser Systems, Inc.K871875MODEL 5050 SURGILASER FOR OB-GYN USELasermatic, Inc.K875314GL-35 COLPOSCOPIC LASER SYSTEMLaser Engineering, Inc.K874615LASER CANNISTER FILTERMedical Marketing, Inc.K880591LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USELaser Peripherals, LLCK880930MDLS 4000,4900,6000,8000,8900 ND:YAG/1700 C02 LASECopper Lasersonics, 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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