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FDA 510(k)

TOURNIQUET PRESSURE REGULATOR

K-Number: K871982 · 1987-06-09

ApplicantAvec Scientific Design Corp.
Decision Date1987-06-09
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TOURNIQUET PRESSURE REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Avec Scientific Design Corp.. It received FDA 510(k) clearance on 1987-06-09 under 510(k) number K871982. The device is classified under product code KCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOURNIQUET PRESSURE REGULATOR?

TOURNIQUET PRESSURE REGULATOR is a medical device that received FDA 510(k) clearance on 1987-06-09. The listed applicant is Avec Scientific Design Corp.. The 510(k) number is K871982.

When did TOURNIQUET PRESSURE REGULATOR receive FDA 510(k) clearance?

TOURNIQUET PRESSURE REGULATOR received FDA 510(k) clearance on 1987-06-09, under 510(k) number K871982.

Who is the listed applicant for TOURNIQUET PRESSURE REGULATOR?

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

What is the FDA product code for TOURNIQUET PRESSURE REGULATOR?

The FDA product code for TOURNIQUET PRESSURE REGULATOR is KCY.

Related Clinical Trials

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.

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Other records listing Avec Scientific Design 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.

K883295CHOP SPINE FRAMEK874494KAMBIN LAMINECTOMY FRAMEK872544IRRIGATION PRESSURE MONITORK871981BILATERAL CONTINUOUS PASSIVE MOTION DEVICEK871900OVER DRAPE LEG HOLDER

Related Devices (Code: KCY)

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.

K202919ATS 5000 Automatic Tourniquet InstrumentMcewen and Associates Consulting , Ltd.K162365T-CuffTerumobct, Inc.K123553ZIMMER A.T.S. 4000TS AUTOMATIC TOURNIQUET SYSTEMZimmer, Inc.K112874EZ VEIN INFLATABLE TOURNIQUETDominion Medical Devices, LLCK071140MRI COMPATIBLE THIGH TOURNIQUET, MODEL C070002Top Spins, Inc.K050411ZIMMER A.T.S. 3000 AUTOMATIC TOURNIQUET SYSTEMZimmer, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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