510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800087Substantially Equivalent

Ultrasonic Flowmeter

Revvity Health Sciences, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800087 is the FDA 510(k) clearance record for ULTRASONIC FLOWMETER, a class I device, cleared for The Perkin-Elmer Corp. on under FDA product code BXP (Transducer, Gas Flow). FDA records list 81 510(k) clearances for Revvity Health Sciences, Inc., from to . As of , FDA records show no recalls naming K800087.

Clearance record

Decision date
Received
(65 days to decision)
Product code
BXP Transducer, Gas Flow
Regulation
21 CFR 868.2885
Device class
Class I
Review panel
Anesthesiology
Applicant
The Perkin-Elmer Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BXP

Trailing 12 months

FDA records hold no clearances under product code BXP in the trailing twelve months.

FDA records show no clearances under product code BXP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BXP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260