510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K970170Substantially Equivalent

Swift Delivery Product #002-Vac Ex Cup W/vac Rel Valve

Richard G. Lindsay, Oklahoma City OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970170 is the FDA 510(k) clearance record for SWIFT DELIVERY PRODUCT #002-VAC EX CUP W/VAC REL VALVE, a class II device, cleared for Richard G. Lindsay on under FDA product code HDB (Extractor, Vacuum, Fetal). FDA records list one 510(k) clearance for Richard G. Lindsay. As of , FDA records show no recalls naming K970170.

Clearance record

Decision date
Received
(78 days to decision)
Product code
HDB Extractor, Vacuum, Fetal
Regulation
21 CFR 884.4340
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Richard G. Lindsay 6824 Elk Canyon Rd., Oklahoma City OK
510(k) summary
Summary
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