FDA 510(k)

PENOX HOSPITAL BED

K-Number: K864667 · 1987-01-21

Decision Date1987-01-21

Product CodeFNJ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PENOX HOSPITAL BED is the device name listed in this FDA 510(k) record. The listed applicant is Penox Technologies, Inc.. It received FDA 510(k) clearance on 1987-01-21 under 510(k) number K864667. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PENOX HOSPITAL BED?

PENOX HOSPITAL BED is a medical device that received FDA 510(k) clearance on 1987-01-21. The listed applicant is Penox Technologies, Inc.. The 510(k) number is K864667.

When did PENOX HOSPITAL BED receive FDA 510(k) clearance?

PENOX HOSPITAL BED received FDA 510(k) clearance on 1987-01-21, under 510(k) number K864667.

Who is the listed applicant for PENOX HOSPITAL BED?

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

What is the FDA product code for PENOX HOSPITAL BED?

The FDA product code for PENOX HOSPITAL BED is FNJ.

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Other records listing Penox Technologies, Inc. as applicant

K863978PORTABLE LIQUID OXYGEN UNIT (MODIFICATION)K862654MODIFIED PENOX LIFT CHAIR K853775PENOX HIGH FLOW MANIFOLD K852109PENOX PERFORMER WHEELCHAIR K851218PENOX LIFT CHAIR K851217PENOX DUAL FLOW MINIFOLD

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Related Devices (Code: FNJ)

K934298KING KRIBNoritage, Inc.K892877CRADLE, HOSPITAL BED CLOTHINGWarsaw Orthopedic, Inc.K885241BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MATKing Mfg. Co.K884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDCommercial Products & Engineering Co.K881725ENVIROTENT (BED)Envirotents, Inc.K881961MSI STANDARD BED MODELS: L1097-64 AND L1085-64Med Service, 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.