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FDA 510(k)

VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600

K-Number: K934482 · 1994-05-02

ApplicantVital Signs, Inc.
Decision Date1994-05-02
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600 is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1994-05-02 under 510(k) number K934482. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600?

VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600 is a medical device that received FDA 510(k) clearance on 1994-05-02. The listed applicant is Vital Signs, Inc.. The 510(k) number is K934482.

When did VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600 receive FDA 510(k) clearance?

VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600 received FDA 510(k) clearance on 1994-05-02, under 510(k) number K934482.

Who is the listed applicant for VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600?

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

What is the FDA product code for VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600?

The FDA product code for VITAL SIGNS DUAL DISPLAY TEMPERATURE MONITOR, MODEL 1600 is FLL.

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Related Devices (Code: FLL)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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