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FDA 510(k)

PATIENT TUBING HYTREL SIEMENS-ELEMA

K-Number: K841657 · 1984-05-23

ApplicantSiemens Elema AB
Decision Date1984-05-23
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PATIENT TUBING HYTREL SIEMENS-ELEMA is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Elema AB. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K841657. 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 PATIENT TUBING HYTREL SIEMENS-ELEMA?

PATIENT TUBING HYTREL SIEMENS-ELEMA is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Siemens Elema AB. The 510(k) number is K841657.

When did PATIENT TUBING HYTREL SIEMENS-ELEMA receive FDA 510(k) clearance?

PATIENT TUBING HYTREL SIEMENS-ELEMA received FDA 510(k) clearance on 1984-05-23, under 510(k) number K841657.

Who is the listed applicant for PATIENT TUBING HYTREL SIEMENS-ELEMA?

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

What is the FDA product code for PATIENT TUBING HYTREL SIEMENS-ELEMA?

The FDA product code for PATIENT TUBING HYTREL SIEMENS-ELEMA is BZO.

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Other records listing Siemens Elema AB 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.

K023354COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EK010923KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392EK010925SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407EK002137CATHCOR DESKTOPK001315MODIFICATION TO KION ANESTHESIA SYSTEMK970839SERVO VENTILATOR 300A

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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.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, 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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