510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K915763Substantially Equivalent

Modified Disposable Fetal Vacuum

Columbia Medical & Surgical, Inc., Bend OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915763 is the FDA 510(k) clearance record for MODIFIED DISPOSABLE FETAL VACUUM, a class II device, cleared for Columbia Medical & Surgical, Inc. on under FDA product code HDB (Extractor, Vacuum, Fetal). FDA records list 4 510(k) clearances for Columbia Medical & Surgical, Inc., from to . As of , FDA records show no recalls naming K915763.

Clearance record

Decision date
Received
(85 days to decision)
Product code
HDB Extractor, Vacuum, Fetal
Regulation
21 CFR 884.4340
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Columbia Medical & Surgical, Inc. P.O. Box 5877, Bend OR
510(k) summary
Statement
Third party review
No

Clearances, product code HDB

Trailing 12 months

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

FDA records show no clearances under product code HDB in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HDB, 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