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FDA 510(k)

MEDCARE REGIONAL ANETHESIA KIT

K-Number: K961075 · 1996-09-06

ApplicantMedcare Medical Group, Inc.
Decision Date1996-09-06
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

MEDCARE REGIONAL ANETHESIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medcare Medical Group, Inc.. It received FDA 510(k) clearance on 1996-09-06 under 510(k) number K961075. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDCARE REGIONAL ANETHESIA KIT?

MEDCARE REGIONAL ANETHESIA KIT is a medical device that received FDA 510(k) clearance on 1996-09-06. The listed applicant is Medcare Medical Group, Inc.. The 510(k) number is K961075.

When did MEDCARE REGIONAL ANETHESIA KIT receive FDA 510(k) clearance?

MEDCARE REGIONAL ANETHESIA KIT received FDA 510(k) clearance on 1996-09-06, under 510(k) number K961075.

Who is the listed applicant for MEDCARE REGIONAL ANETHESIA KIT?

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

What is the FDA product code for MEDCARE REGIONAL ANETHESIA KIT?

The FDA product code for MEDCARE REGIONAL ANETHESIA KIT is CAZ.

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Other records listing Medcare Medical Group, 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.

K973497HUBERLOCK970152BIOPSY TRAYK962849CATHETER INSERTION TRAYK962328SINGLE USE INSTRUMENT TRAYK962527GENERAL PURPOSE DENTAL TRAYK961880MEDCARE SUCTION CONNECTING TUBING

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Related Devices (Code: CAZ)

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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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