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FDA 510(k)

WISP MODEL 710

K-Number: K772311 · 1978-01-12

ApplicantWaters Assoc., Inc.
Decision Date1978-01-12
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WISP MODEL 710 is the device name listed in this FDA 510(k) record. The listed applicant is Waters Assoc., Inc.. It received FDA 510(k) clearance on 1978-01-12 under 510(k) number K772311. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WISP MODEL 710?

WISP MODEL 710 is a medical device that received FDA 510(k) clearance on 1978-01-12. The listed applicant is Waters Assoc., Inc.. The 510(k) number is K772311.

When did WISP MODEL 710 receive FDA 510(k) clearance?

WISP MODEL 710 received FDA 510(k) clearance on 1978-01-12, under 510(k) number K772311.

Who is the listed applicant for WISP MODEL 710?

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

What is the FDA product code for WISP MODEL 710?

The FDA product code for WISP MODEL 710 is CHH.

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Other records listing Waters Assoc., Inc. as applicant

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K811975MODEL 480 VARIABLE WAVELENGTH ULTRA VIOLK8024817FRENCH FLOW DIRECTED TRIPLE LUMEN CATHK801852MRM-2 OXYGEN CONSUMPTION MONITORK801431PAN-AM MYELOGRAM TRAYK791661SYSTEM CONTROLLER 720 SERIESK7910264F STERILE BALLOON-LESS, CATHETER 913-28

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Related Devices (Code: CHH)

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K251091LipidsTruvian HealthK232404CHOLESTEROL; HDL-cholesterol ; LDL-cholesterol; TRIGLYCERIDESMedicon Hellas S.AK203597Cholesterol2Abbott Ireland Diagnostics DivisionK190490VITROS XT Chemistry Products TRIG-CHOL SlidesOrtho-Clinical Diagnostics, Inc.K181373Extended Lipid Panel AssayLaboratory Corporation of America HoldingsK180504Mission Lipid Panel Monitoring SystemACON Laboratories, 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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