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FDA 510(k)

LIBERATOR/STROLLER

K-Number: K760787 · 1976-10-22

ApplicantBurditt & Calkins-Siemens-Elema
Decision Date1976-10-22
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIBERATOR/STROLLER is the device name listed in this FDA 510(k) record. The listed applicant is Burditt & Calkins-Siemens-Elema. It received FDA 510(k) clearance on 1976-10-22 under 510(k) number K760787. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERATOR/STROLLER?

LIBERATOR/STROLLER is a medical device that received FDA 510(k) clearance on 1976-10-22. The listed applicant is Burditt & Calkins-Siemens-Elema. The 510(k) number is K760787.

When did LIBERATOR/STROLLER receive FDA 510(k) clearance?

LIBERATOR/STROLLER received FDA 510(k) clearance on 1976-10-22, under 510(k) number K760787.

Who is the listed applicant for LIBERATOR/STROLLER?

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

What is the FDA product code for LIBERATOR/STROLLER?

The FDA product code for LIBERATOR/STROLLER is BYJ.

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Other records listing Burditt & Calkins-Siemens-Elema as applicant

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K833519PULSE GENERATOR MODEL 688K833155RAYDEN MEDICAL MINI PULSE VOLUME RECORDK830344SIEMENS-ELMA PULSE GENERATOR #718K823435MON-A-THERM MYOCARDIAL TEMP. SENSORK823591AMEDA HAND BREAST PUMPK822239COAXIAL BIPOLAR PACING ELECTRODE

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Related Devices (Code: BYJ)

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.

K130068DISMOUNTED MEDICAL & SUPPLEMENTAL OXYGEN SYSTEM (DMOS)Essex Industries, Inc. D/B/A Essex Cryogenics of MK113767MOUNTED MEDICAL OXYGEN SYSTEMEssex Industries, Inc.K103324PRECISION LIQUID OXYGEN SYSTEMPrecision Medical, Inc.K101272MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3Essex Industries, Inc.K081779GOLOX-93Respironics, Inc.K080023MODIFICATION TO: SPIRITCaire, 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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