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FDA 510(k)

FLOCARE DRY CAS SAMPLING PORT MODELS

K-Number: K912700 · 1991-09-11

ApplicantFlocare Medical
Decision Date1991-09-11
Product CodeBYD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FLOCARE DRY CAS SAMPLING PORT MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Flocare Medical. It received FDA 510(k) clearance on 1991-09-11 under 510(k) number K912700. The device is classified under product code BYD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOCARE DRY CAS SAMPLING PORT MODELS?

FLOCARE DRY CAS SAMPLING PORT MODELS is a medical device that received FDA 510(k) clearance on 1991-09-11. The listed applicant is Flocare Medical. The 510(k) number is K912700.

When did FLOCARE DRY CAS SAMPLING PORT MODELS receive FDA 510(k) clearance?

FLOCARE DRY CAS SAMPLING PORT MODELS received FDA 510(k) clearance on 1991-09-11, under 510(k) number K912700.

Who is the listed applicant for FLOCARE DRY CAS SAMPLING PORT MODELS?

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

What is the FDA product code for FLOCARE DRY CAS SAMPLING PORT MODELS?

The FDA product code for FLOCARE DRY CAS SAMPLING PORT MODELS is BYD.

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 Flocare Medical 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.

K912699FLOCARE LF-AK904193FLOCAREK903404FLOCARE FK902501FLOCARE N

Related Devices (Code: BYD)

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.

K955008HEAT & MOISTURE EXCHANGERIntertech Resources, Inc.K954194DISPOSABLE HME/FILTEREngstrom MedicalK953580HEAT MOISTURE EXCHANGERIntertech Resources, Inc.K953507TYPE 1 & 2 (HUMIDAIR I & II)Icor ABK953544HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHTGibeck, Inc.K953620WARM N WET HMEF W/LUER ADAPTERHospitak, 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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