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FDA 510(k)

ADULT FLEXFLOAT

K-Number: K812684 · 1981-10-08

ApplicantPharmaquest Corp.
Decision Date1981-10-08
Product CodeFOH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADULT FLEXFLOAT is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaquest Corp.. It received FDA 510(k) clearance on 1981-10-08 under 510(k) number K812684. The device is classified under product code FOH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT FLEXFLOAT?

ADULT FLEXFLOAT is a medical device that received FDA 510(k) clearance on 1981-10-08. The listed applicant is Pharmaquest Corp.. The 510(k) number is K812684.

When did ADULT FLEXFLOAT receive FDA 510(k) clearance?

ADULT FLEXFLOAT received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812684.

Who is the listed applicant for ADULT FLEXFLOAT?

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

What is the FDA product code for ADULT FLEXFLOAT?

The FDA product code for ADULT FLEXFLOAT is FOH.

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Related Devices (Code: FOH)

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.

K954216OLYMPIC WARM-BASSINETOlympic Medical Corp.K872876IMSI/EASY FLOAT MATTRESSIntl. Management Services, Inc.K812683NEONATE FLEXFLOATPharmaquest Corp.K812682FLEXFLOAT HEATERPharmaquest Corp.K812681ADULT FLEX FLOAT W/HEATERPharmaquest Corp.

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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