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FDA 510(k)

MODEL 52 BUNN DRY AIR SUPPLY

K-Number: K800534 · 1980-03-25

ApplicantGreene & Kellogg, Inc.
Decision Date1980-03-25
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 52 BUNN DRY AIR SUPPLY is the device name listed in this FDA 510(k) record. The listed applicant is Greene & Kellogg, Inc.. It received FDA 510(k) clearance on 1980-03-25 under 510(k) number K800534. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 52 BUNN DRY AIR SUPPLY?

MODEL 52 BUNN DRY AIR SUPPLY is a medical device that received FDA 510(k) clearance on 1980-03-25. The listed applicant is Greene & Kellogg, Inc.. The 510(k) number is K800534.

When did MODEL 52 BUNN DRY AIR SUPPLY receive FDA 510(k) clearance?

MODEL 52 BUNN DRY AIR SUPPLY received FDA 510(k) clearance on 1980-03-25, under 510(k) number K800534.

Who is the listed applicant for MODEL 52 BUNN DRY AIR SUPPLY?

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

What is the FDA product code for MODEL 52 BUNN DRY AIR SUPPLY?

The FDA product code for MODEL 52 BUNN DRY AIR SUPPLY is BTI.

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 Greene & Kellogg, 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.

K833495BUNN MICRO OXYGEN CONCENTRATORK830046MODEL HI-FLO2 OXYGEN RICH AIR SUPPLYK811155MODEL RXO2 OXYGEN RICH AIR SUPPLY

Related Devices (Code: BTI)

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.

K131881OMBRA TABLE TOP COMPRESSORTrudell Medical Intl.K113338MEDICAL AIR COMPRESSOROricare, Inc.K091871DK50 DSEkom S.R.O.K072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESEmg Technology Co., Ltd.K060781MEDICAL COMPRESSOR, MODELS DK50 D AND DMEkom S.R.O.K051691MINIMATE COMPRESSORPrecision Medical, Inc.

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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