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FDA 510(k)

BED ROCKING DEVICE

K-Number: K801517 · 1980-10-10

ApplicantWesler
Decision Date1980-10-10
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BED ROCKING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Wesler. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K801517. 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 BED ROCKING DEVICE?

BED ROCKING DEVICE is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Wesler. The 510(k) number is K801517.

When did BED ROCKING DEVICE receive FDA 510(k) clearance?

BED ROCKING DEVICE received FDA 510(k) clearance on 1980-10-10, under 510(k) number K801517.

Who is the listed applicant for BED ROCKING DEVICE?

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

What is the FDA product code for BED ROCKING DEVICE?

The FDA product code for BED ROCKING DEVICE is FNJ.

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Related Devices (Code: FNJ)

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.

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.

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