510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K933848Substantially Equivalent

Prespo 7, Self-Sufficient Drip Device

Bonding Corp., Coraopolis PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933848 is the FDA 510(k) clearance record for PRESPO 7, SELF-SUFFICIENT DRIP DEVICE, a class II device, cleared for Bonding Corp. on under FDA product code FPA (Set, Administration, Intravascular). FDA records list one 510(k) clearance for Bonding Corp. As of , FDA records show no recalls naming K933848.

Clearance record

Decision date
Received
(574 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Bonding Corp. 429 Moon Clinton Rd., Coraopolis PA
510(k) summary
Statement
Third party review
No

Clearances, product code FPA

Trailing 12 months
5 clearances under product code FPA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FPA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260