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FDA 510(k)

VAN DELLEN ASPIRATOR

K-Number: K873462 · 1987-09-25

ApplicantVan Dellen, Ltd.
Decision Date1987-09-25
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VAN DELLEN ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Van Dellen, Ltd.. It received FDA 510(k) clearance on 1987-09-25 under 510(k) number K873462. 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 VAN DELLEN ASPIRATOR?

VAN DELLEN ASPIRATOR is a medical device that received FDA 510(k) clearance on 1987-09-25. The listed applicant is Van Dellen, Ltd.. The 510(k) number is K873462.

When did VAN DELLEN ASPIRATOR receive FDA 510(k) clearance?

VAN DELLEN ASPIRATOR received FDA 510(k) clearance on 1987-09-25, under 510(k) number K873462.

Who is the listed applicant for VAN DELLEN ASPIRATOR?

The FDA 510(k) record lists Van Dellen, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAN DELLEN ASPIRATOR?

The FDA product code for VAN DELLEN 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.

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Other records listing Van Dellen, Ltd. 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.

K873465VAN DELLEN BACTERIA FILTERK873463VAN DELLEN ASPIRATING TUBINGK873464VAN DELLEN CANNULAK873164VAN DELLEN HEALON CANNULAK873162VAN DELLEN RETROBULBAR NEEDLEK873163VAN DELLEN IRRIGATING CYSTOTOME

View all 7 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.

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