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FDA 510(k)

FLEXFLOAT HEATER

K-Number: K812682 · 1981-10-08

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

Device Summary

FLEXFLOAT 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 K812682. 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 FLEXFLOAT HEATER?

FLEXFLOAT 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 K812682.

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

FLEXFLOAT HEATER received FDA 510(k) clearance on 1981-10-08, under 510(k) number K812682.

Who is the listed applicant for FLEXFLOAT 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 FLEXFLOAT HEATER?

The FDA product code for FLEXFLOAT 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.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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