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FDA 510(k)

CAM-10 RESPIRATORY HOSE ASSEMBLIES

K-Number: K801859 · 1980-09-09

ApplicantLifecare Services, Inc.
Decision Date1980-09-09
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAM-10 RESPIRATORY HOSE ASSEMBLIES is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare Services, Inc.. It received FDA 510(k) clearance on 1980-09-09 under 510(k) number K801859. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAM-10 RESPIRATORY HOSE ASSEMBLIES?

CAM-10 RESPIRATORY HOSE ASSEMBLIES is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Lifecare Services, Inc.. The 510(k) number is K801859.

When did CAM-10 RESPIRATORY HOSE ASSEMBLIES receive FDA 510(k) clearance?

CAM-10 RESPIRATORY HOSE ASSEMBLIES received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801859.

Who is the listed applicant for CAM-10 RESPIRATORY HOSE ASSEMBLIES?

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

What is the FDA product code for CAM-10 RESPIRATORY HOSE ASSEMBLIES?

The FDA product code for CAM-10 RESPIRATORY HOSE ASSEMBLIES is BZO.

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Other records listing Lifecare Services, 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.

K913423LIFECARE REMOTE ALARM IIK912224LIFECARE CPAP-100K910947NEV-10 NEGATIVE PRESSURE VENTILATORK894779LIFECARE NASAL MASK KIT CAT. NO. 06-800K895592FREEWAY NEBULIZER COMPRESSORK894361LIFECARE PRESSURE ALARM CAT. NO. 34-010

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Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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