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FDA 510(k)

DEVIN-NESTOR PNEUMATIC TOURNIQUET

K-Number: K780988 · 1978-10-03

ApplicantNestor Engineering Associates, Inc.
Decision Date1978-10-03
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEVIN-NESTOR PNEUMATIC TOURNIQUET is the device name listed in this FDA 510(k) record. The listed applicant is Nestor Engineering Associates, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K780988. 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 DEVIN-NESTOR PNEUMATIC TOURNIQUET?

DEVIN-NESTOR PNEUMATIC TOURNIQUET is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Nestor Engineering Associates, Inc.. The 510(k) number is K780988.

When did DEVIN-NESTOR PNEUMATIC TOURNIQUET receive FDA 510(k) clearance?

DEVIN-NESTOR PNEUMATIC TOURNIQUET received FDA 510(k) clearance on 1978-10-03, under 510(k) number K780988.

Who is the listed applicant for DEVIN-NESTOR PNEUMATIC TOURNIQUET?

The FDA 510(k) record lists Nestor Engineering Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVIN-NESTOR PNEUMATIC TOURNIQUET?

The FDA product code for DEVIN-NESTOR PNEUMATIC TOURNIQUET 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 Nestor Engineering Associates, Inc. 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.

K780990STAINLESS STEEL TEMPLATEK780991PARALLEL BLADE MARKERK780989DEVIN-NESTOR SQUARE KNIFEK780992MILLARD MOUTH GAG

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

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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