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FDA 510(k)

SERIES 2000 ADJUSTABLE BED

K-Number: K903904 · 1990-10-12

ApplicantEqui-Tron Mfg., Inc.
Decision Date1990-10-12
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SERIES 2000 ADJUSTABLE BED is the device name listed in this FDA 510(k) record. The listed applicant is Equi-Tron Mfg., Inc.. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K903904. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 2000 ADJUSTABLE BED?

SERIES 2000 ADJUSTABLE BED is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Equi-Tron Mfg., Inc.. The 510(k) number is K903904.

When did SERIES 2000 ADJUSTABLE BED receive FDA 510(k) clearance?

SERIES 2000 ADJUSTABLE BED received FDA 510(k) clearance on 1990-10-12, under 510(k) number K903904.

Who is the listed applicant for SERIES 2000 ADJUSTABLE BED?

The FDA 510(k) record lists Equi-Tron Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 2000 ADJUSTABLE BED?

The FDA product code for SERIES 2000 ADJUSTABLE BED is FNL.

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 Equi-Tron Mfg., 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.

K9627632000 MODULAR THIRTY-NINEK903905SERIES 9000 LIFT-RECLINE CHAIRK902089EQUI-GUARD (ASPIRATOR FILTER)K894831PORTABLE AIR COMPRESSOR MODEL NUMBER 8125

Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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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