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FDA 510(k)

ADULT FLEX FLOAT W/HEATER

K-Number: K812681 · 1981-10-08

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

Device Summary

ADULT FLEX FLOAT W/HEATER 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 K812681. 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 FLEX FLOAT W/HEATER?

ADULT FLEX FLOAT W/HEATER 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 K812681.

When did ADULT FLEX FLOAT W/HEATER receive FDA 510(k) clearance?

ADULT FLEX FLOAT W/HEATER received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812681.

Who is the listed applicant for ADULT FLEX FLOAT W/HEATER?

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 FLEX FLOAT W/HEATER?

The FDA product code for ADULT FLEX FLOAT W/HEATER 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.K812684ADULT FLEXFLOATPharmaquest Corp.K812682FLEXFLOAT 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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