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FDA 510(k)

NITROUS OXIDE RECYCLER

K-Number: K834535 · 1984-06-07

ApplicantG & L Unltd.
Decision Date1984-06-07
Product CodeBSF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NITROUS OXIDE RECYCLER is the device name listed in this FDA 510(k) record. The listed applicant is G & L Unltd.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K834535. The device is classified under product code BSF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NITROUS OXIDE RECYCLER?

NITROUS OXIDE RECYCLER is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is G & L Unltd.. The 510(k) number is K834535.

When did NITROUS OXIDE RECYCLER receive FDA 510(k) clearance?

NITROUS OXIDE RECYCLER received FDA 510(k) clearance on 1984-06-07, under 510(k) number K834535.

Who is the listed applicant for NITROUS OXIDE RECYCLER?

The FDA 510(k) record lists G & L Unltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NITROUS OXIDE RECYCLER?

The FDA product code for NITROUS OXIDE RECYCLER is BSF.

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Related Devices (Code: BSF)

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.

K951093KAB SYSTEMKing Systems Corp.K852071OHMEDA GMS ABOSORBEROhmeda MedicalK843422OHMEDA BAIN CIRCUIT ADAPTER GMS ABSOROhmeda MedicalK833452OHIO GMS ABSORBERAirco/Ohio Medical ProductsK821144OHIO ABSORBEROhio Medical ProductsK801255PENLON JUMBO CARBON DIOXIDE ABSORBERPenlon, 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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