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FDA 510(k)

BUNN MODEL 530 ASPIRATOR

K-Number: K870094 · 1987-03-06

ApplicantThe John Bunn Co.
Decision Date1987-03-06
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BUNN MODEL 530 ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is The John Bunn Co.. It received FDA 510(k) clearance on 1987-03-06 under 510(k) number K870094. 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 BUNN MODEL 530 ASPIRATOR?

BUNN MODEL 530 ASPIRATOR is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is The John Bunn Co.. The 510(k) number is K870094.

When did BUNN MODEL 530 ASPIRATOR receive FDA 510(k) clearance?

BUNN MODEL 530 ASPIRATOR received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870094.

Who is the listed applicant for BUNN MODEL 530 ASPIRATOR?

The FDA 510(k) record lists The John Bunn Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUNN MODEL 530 ASPIRATOR?

The FDA product code for BUNN MODEL 530 ASPIRATOR is BTA.

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Other records listing The John Bunn Co. 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.

K900854JOHN BUNN: MEDIX COMPACT TRAVELLERK883216BUNN MODEL 50 OXYGEN FLOW CONTROLLERK873071BUNN CONCENTRATOR MODEL 2100 SERIESK861435BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVEK861199BUNN MODEL 22 OXYGEN FLOW CONTROLLERK862628BUNN MODEL 510 MEDICATION COMPRESSOR

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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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