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FDA 510(k)

ANTIMICROBIAL AND SINGLE-PATIENT CUFFS

K-Number: K071885 · 2007-12-20

ApplicantPhilips Medical Systems
Decision Date2007-12-20
Product CodeOED
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANTIMICROBIAL AND SINGLE-PATIENT CUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2007-12-20 under 510(k) number K071885. The device is classified under product code OED. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTIMICROBIAL AND SINGLE-PATIENT CUFFS?

ANTIMICROBIAL AND SINGLE-PATIENT CUFFS is a medical device that received FDA 510(k) clearance on 2007-12-20. The listed applicant is Philips Medical Systems. The 510(k) number is K071885.

When did ANTIMICROBIAL AND SINGLE-PATIENT CUFFS receive FDA 510(k) clearance?

ANTIMICROBIAL AND SINGLE-PATIENT CUFFS received FDA 510(k) clearance on 2007-12-20, under 510(k) number K071885.

Who is the listed applicant for ANTIMICROBIAL AND SINGLE-PATIENT CUFFS?

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

What is the FDA product code for ANTIMICROBIAL AND SINGLE-PATIENT CUFFS?

The FDA product code for ANTIMICROBIAL AND SINGLE-PATIENT CUFFS is OED.

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Other records listing Philips Medical Systems as applicant

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.

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Related Devices (Code: OED)

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.

K122365ULTRACHECK CURVE BLOOD PRESSURE CUFFSStatcorp Medical

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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