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FDA 510(k)

BD6000 THE OPTIMA & BD5000 BIRTHING BED

K-Number: K914544 · 1993-11-24

ApplicantLic Care, Inc.
Decision Date1993-11-24
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BD6000 THE OPTIMA & BD5000 BIRTHING BED is the device name listed in this FDA 510(k) record. The listed applicant is Lic Care, Inc.. It received FDA 510(k) clearance on 1993-11-24 under 510(k) number K914544. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD6000 THE OPTIMA & BD5000 BIRTHING BED?

BD6000 THE OPTIMA & BD5000 BIRTHING BED is a medical device that received FDA 510(k) clearance on 1993-11-24. The listed applicant is Lic Care, Inc.. The 510(k) number is K914544.

When did BD6000 THE OPTIMA & BD5000 BIRTHING BED receive FDA 510(k) clearance?

BD6000 THE OPTIMA & BD5000 BIRTHING BED received FDA 510(k) clearance on 1993-11-24, under 510(k) number K914544.

Who is the listed applicant for BD6000 THE OPTIMA & BD5000 BIRTHING BED?

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

What is the FDA product code for BD6000 THE OPTIMA & BD5000 BIRTHING BED?

The FDA product code for BD6000 THE OPTIMA & BD5000 BIRTHING BED is KNC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Lic Care, 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.

K914543ST5500 UNIVERSAL CARE STRETCHER

Related Devices (Code: KNC)

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.

K001261L720 EXAMINATION CHAIRLuneau Gynecologie SAK932035NON-LINTING DELIVERY BLANKETAmsco Sterile Recoveries, Inc.K924420MEDICAL DISPOSABLE BEDDINGHill-Rom, Inc.K915779AFFINITY BED MODEL 3600 SERIESHill-Rom, Inc.K903973GARDOSI BIRTHING CUSHIONGraphic Controls Corp.K884868OBSTETRICAL SAFETY SYSTEMBuckman Co., Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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