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FDA 510(k)

CAPILLARY ADAPTOR ACCESSORY

K-Number: K963992 · 1996-11-29

ApplicantMedica Corp.
Decision Date1996-11-29
Product CodeCGZ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CAPILLARY ADAPTOR ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Medica Corp.. It received FDA 510(k) clearance on 1996-11-29 under 510(k) number K963992. The device is classified under product code CGZ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPILLARY ADAPTOR ACCESSORY?

CAPILLARY ADAPTOR ACCESSORY is a medical device that received FDA 510(k) clearance on 1996-11-29. The listed applicant is Medica Corp.. The 510(k) number is K963992.

When did CAPILLARY ADAPTOR ACCESSORY receive FDA 510(k) clearance?

CAPILLARY ADAPTOR ACCESSORY received FDA 510(k) clearance on 1996-11-29, under 510(k) number K963992.

Who is the listed applicant for CAPILLARY ADAPTOR ACCESSORY?

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

What is the FDA product code for CAPILLARY ADAPTOR ACCESSORY?

The FDA product code for CAPILLARY ADAPTOR ACCESSORY is CGZ.

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 Medica 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.

View all 47 devices →

Related Devices (Code: CGZ)

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

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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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