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FDA 510(k)

CAPILLARY SAMPLE LINE

K-Number: K771516 · 1977-08-16

ApplicantMcgaw Respiratory Therapy
Decision Date1977-08-16
Product CodeCCI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPILLARY SAMPLE LINE is the device name listed in this FDA 510(k) record. The listed applicant is Mcgaw Respiratory Therapy. It received FDA 510(k) clearance on 1977-08-16 under 510(k) number K771516. The device is classified under product code CCI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPILLARY SAMPLE LINE?

CAPILLARY SAMPLE LINE is a medical device that received FDA 510(k) clearance on 1977-08-16. The listed applicant is Mcgaw Respiratory Therapy. The 510(k) number is K771516.

When did CAPILLARY SAMPLE LINE receive FDA 510(k) clearance?

CAPILLARY SAMPLE LINE received FDA 510(k) clearance on 1977-08-16, under 510(k) number K771516.

Who is the listed applicant for CAPILLARY SAMPLE LINE?

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

What is the FDA product code for CAPILLARY SAMPLE LINE?

The FDA product code for CAPILLARY SAMPLE LINE is CCI.

Related Clinical Trials

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Other records listing Mcgaw Respiratory Therapy 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.

K771550MRT DISPENSORK770665VALVE, PRESSURE, DEMANDK770286VENTILATOR BREATHING CIRCUITK761299DISPOSABLE NEBULIZERK761300NEBULIZER CONTROL UNITK761298PRE-FILLED DISPOSABLE NEBULIZER

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Related Devices (Code: CCI)

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.

K872024CO2/02 MONITOR MULTINEXDatascope Corp.

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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