Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Model 330 Multifunction Aspirator

K-Number: K170533 · 2017-04-18

ApplicantZOLL Medical Corporation
Decision Date2017-04-18
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Model 330 Multifunction Aspirator is the device name listed in this FDA 510(k) record. The listed applicant is ZOLL Medical Corporation. It received FDA 510(k) clearance on 2017-04-18 under 510(k) number K170533. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Model 330 Multifunction Aspirator?

Model 330 Multifunction Aspirator is a medical device that received FDA 510(k) clearance on 2017-04-18. The listed applicant is ZOLL Medical Corporation. The 510(k) number is K170533.

When did Model 330 Multifunction Aspirator receive FDA 510(k) clearance?

Model 330 Multifunction Aspirator received FDA 510(k) clearance on 2017-04-18, under 510(k) number K170533.

Who is the listed applicant for Model 330 Multifunction Aspirator?

The FDA 510(k) record lists ZOLL Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Model 330 Multifunction Aspirator?

The FDA product code for Model 330 Multifunction Aspirator is BTA.

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.

NCT07622472Remote Monitoring and Optimization of Heart Failure TherapyNOT_YET_RECRUITING

Other records listing ZOLL Medical Corporation 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.

PMA P160015Automated external defibrillators (non-wearable)PMA P160022Automated external defibrillators (non-wearable)PMA P160033Automated external defibrillators (non-wearable)PMA P890057VENTILATOR, HIGH FREQUENCYK233486731 Series VentilatorPMA P110024Combination compression/decompression manual chest pump with impedance respiratory valve

View all 12 devices →

Related Devices (Code: BTA)

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.

K253629Momcozy Nasal Aspirator (BN007)Shenzhen Root Innovation Technology Co., Ltd.K260134Baby Nasal Aspirator (BN006, BN006-A, BN006-B, BN006-C, BN006-D, BN02; BN008, BN008-A, BN008-B, BN008-C, BN008-D, BC-021)Shenzhen Root Innovation Technology Co., Ltd.K260892Suction Pump (SU-90)Shenzhen HugeMed Medical Technical Development Co., Ltd.K260473Electric nasal aspirator (BC027, BC030, BC033, BC035, BC035B)Shenzhen Kingboom Technology Co., Ltd.K253107Electric Nasal Aspirator (DT10 and DT50, DX80, DX85, DX86 and DX90)Shenzhen Dongjiang Technology Co., Ltd.K260147Electric nasal aspirator (BC026, BC025, BC023, BC028, BC029, BC036)Shenzhen Kingboom Technology Co., Ltd.

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.

↑