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FDA 510(k)

MEDCARE SUCTION CONNECTING TUBING

K-Number: K961880 · 1996-07-19

Decision Date1996-07-19
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDCARE SUCTION CONNECTING TUBING 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 1996-07-19 under 510(k) number K961880. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDCARE SUCTION CONNECTING TUBING?

MEDCARE SUCTION CONNECTING TUBING is a medical device that received FDA 510(k) clearance on 1996-07-19. The listed applicant is Medcare Medical Group, Inc.. The 510(k) number is K961880.

When did MEDCARE SUCTION CONNECTING TUBING receive FDA 510(k) clearance?

MEDCARE SUCTION CONNECTING TUBING received FDA 510(k) clearance on 1996-07-19, under 510(k) number K961880.

Who is the listed applicant for MEDCARE SUCTION CONNECTING TUBING?

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 SUCTION CONNECTING TUBING?

The FDA product code for MEDCARE SUCTION CONNECTING TUBING is GCX.

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.

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.

View all 8 devices →

Related Devices (Code: GCX)

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.

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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