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FDA 510(k)

DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET

K-Number: K870046 · 1987-03-05

ApplicantTti Medical
Decision Date1987-03-05
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET is the device name listed in this FDA 510(k) record. The listed applicant is Tti Medical. It received FDA 510(k) clearance on 1987-03-05 under 510(k) number K870046. 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 DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET?

DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET is a medical device that received FDA 510(k) clearance on 1987-03-05. The listed applicant is Tti Medical. The 510(k) number is K870046.

When did DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET receive FDA 510(k) clearance?

DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET received FDA 510(k) clearance on 1987-03-05, under 510(k) number K870046.

Who is the listed applicant for DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET?

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

What is the FDA product code for DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET?

The FDA product code for DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET is HHR.

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Other records listing Tti Medical 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.

K952006ACCU-BEAM FIBER OPTIC HANDPIECEK951895ACCU-BEAM 300W XENON LIGHT SOURCEK945648ACCU-BEAM C02 LASER HANDPIECEK921208ACCU-BEAM TUBE SETK910978ACCU-BEAM LAPAROSCOPIC SYSTEMK895656ACCU-BEAM WAVEGUIDE

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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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