FDA 510(k)

MODEL 172-P AND 172-N ROTARY SPRAY ARM

K-Number: K882465 · 1988-06-24

ApplicantBoling Precision Components Co.

Decision Date1988-06-24

Product CodeFLE

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MODEL 172-P AND 172-N ROTARY SPRAY ARM is the device name listed in this FDA 510(k) record. The listed applicant is Boling Precision Components Co.. It received FDA 510(k) clearance on 1988-06-24 under 510(k) number K882465. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 172-P AND 172-N ROTARY SPRAY ARM?

MODEL 172-P AND 172-N ROTARY SPRAY ARM is a medical device that received FDA 510(k) clearance on 1988-06-24. The listed applicant is Boling Precision Components Co.. The 510(k) number is K882465.

When did MODEL 172-P AND 172-N ROTARY SPRAY ARM receive FDA 510(k) clearance?

MODEL 172-P AND 172-N ROTARY SPRAY ARM received FDA 510(k) clearance on 1988-06-24, under 510(k) number K882465.

Who is the listed applicant for MODEL 172-P AND 172-N ROTARY SPRAY ARM?

The FDA 510(k) record lists Boling Precision Components Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 172-P AND 172-N ROTARY SPRAY ARM?

The FDA product code for MODEL 172-P AND 172-N ROTARY SPRAY ARM is FLE.

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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.