FDA 510(k)

ULTRASOUND LINEAR/SECTOR SCANNER 1100

K-Number: K870653 · 1988-02-02

Decision Date1988-02-02

Product CodeKNG

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

ULTRASOUND LINEAR/SECTOR SCANNER 1100 is the device name listed in this FDA 510(k) record. The listed applicant is Pie Data Medical BV. It received FDA 510(k) clearance on 1988-02-02 under 510(k) number K870653. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASOUND LINEAR/SECTOR SCANNER 1100?

ULTRASOUND LINEAR/SECTOR SCANNER 1100 is a medical device that received FDA 510(k) clearance on 1988-02-02. The listed applicant is Pie Data Medical BV. The 510(k) number is K870653.

When did ULTRASOUND LINEAR/SECTOR SCANNER 1100 receive FDA 510(k) clearance?

ULTRASOUND LINEAR/SECTOR SCANNER 1100 received FDA 510(k) clearance on 1988-02-02, under 510(k) number K870653.

Who is the listed applicant for ULTRASOUND LINEAR/SECTOR SCANNER 1100?

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

What is the FDA product code for ULTRASOUND LINEAR/SECTOR SCANNER 1100?

The FDA product code for ULTRASOUND LINEAR/SECTOR SCANNER 1100 is KNG.

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Other records listing Pie Data Medical BV as applicant

K874192MULTIPURPOSE TRANSDUCER RANGE K870058PIE MEDICAL SCANNER 1000 K874081ENTERSCAN K871082FETAL CARE MONITOR ANTEPARTUM 1500

Related Devices (Code: KNG)

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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.