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FDA 510(k)

SWIFT DELIVERY PRODUCT #300

K-Number: K973942 · 1997-12-12

ApplicantSwift Delivery Products
Decision Date1997-12-12
Product CodeHDB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SWIFT DELIVERY PRODUCT #300 is the device name listed in this FDA 510(k) record. The listed applicant is Swift Delivery Products. It received FDA 510(k) clearance on 1997-12-12 under 510(k) number K973942. The device is classified under product code HDB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SWIFT DELIVERY PRODUCT #300?

SWIFT DELIVERY PRODUCT #300 is a medical device that received FDA 510(k) clearance on 1997-12-12. The listed applicant is Swift Delivery Products. The 510(k) number is K973942.

When did SWIFT DELIVERY PRODUCT #300 receive FDA 510(k) clearance?

SWIFT DELIVERY PRODUCT #300 received FDA 510(k) clearance on 1997-12-12, under 510(k) number K973942.

Who is the listed applicant for SWIFT DELIVERY PRODUCT #300?

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

What is the FDA product code for SWIFT DELIVERY PRODUCT #300?

The FDA product code for SWIFT DELIVERY PRODUCT #300 is HDB.

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 Swift Delivery Products 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.

K013460SWIFT LOW PROFILE CUP (PRO CUP)K963287VACUUM CUP (004SD)

Related Devices (Code: HDB)

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.

K250298Kiwi® Complete Vacuum Delivery System, OmniCup® (VAC-DUAL M); Kiwi® Complete Vacuum Delivery System, OmniCup® with Traction Force Indicator (VAC-DUAL MT); Kiwi® Complete Vacuum Delivery System, OmniC Cup® for Cesarean Section (VAC-DUAL C); Kiwi® Complete Vacuum Delivery System, ProCup® (VAC-DUAL S)Clinical Innovations, LLCK041579MEDELA SINGLE USE SILC CUP, MODEL 077.0791Medela AGK043614VACULINK, MODEL VCL 3000Medevco, Inc.K021193FORTUNE SILICONE VACUUM SUCTION, MODEL #1300Fortune Medical Instrument Corp.K020447MITYVAC MERLIN, MODEL 10027Prism Enterprises, Inc.K013460SWIFT LOW PROFILE CUP (PRO CUP)Swift Delivery Products

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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