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FDA 510(k)

ABDOMINAL PRESSURE CONTROL VALVE

K-Number: K844829 · 1985-05-01

ApplicantL.A.S.E.R., Inc.
Decision Date1985-05-01
Product CodeHHR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ABDOMINAL PRESSURE CONTROL VALVE is the device name listed in this FDA 510(k) record. The listed applicant is L.A.S.E.R., Inc.. It received FDA 510(k) clearance on 1985-05-01 under 510(k) number K844829. 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 ABDOMINAL PRESSURE CONTROL VALVE?

ABDOMINAL PRESSURE CONTROL VALVE is a medical device that received FDA 510(k) clearance on 1985-05-01. The listed applicant is L.A.S.E.R., Inc.. The 510(k) number is K844829.

When did ABDOMINAL PRESSURE CONTROL VALVE receive FDA 510(k) clearance?

ABDOMINAL PRESSURE CONTROL VALVE received FDA 510(k) clearance on 1985-05-01, under 510(k) number K844829.

Who is the listed applicant for ABDOMINAL PRESSURE CONTROL VALVE?

The FDA 510(k) record lists L.A.S.E.R., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABDOMINAL PRESSURE CONTROL VALVE?

The FDA product code for ABDOMINAL PRESSURE CONTROL VALVE is HHR.

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Other records listing L.A.S.E.R., Inc. as applicant

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K983965CO2 LASER COUPLERK950021REUSABLE TROCAR WITH SAFETY SLEEVEK940454GRASPING FORCEPS, PUNCHES, SCISSORSK931561TROCAR SLEEVEK933421ENDOSCOPIC INSTRUMENTS AND ACCESSDORIESK924844BULK TISSUE REMOVAL SYSTEM

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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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