510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K101141Substantially Equivalent

Seiler Colposcope, Models 935, 955 and 985

Seiler Precision Microscopes, St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K101141 is the FDA 510(k) clearance record for SEILER COLPOSCOPE, MODELS 935, 955 AND 985, a class II device, cleared for Seiler Precision Microscopes on under FDA product code HEX (Colposcope (And Colpomicroscope)). FDA records list one 510(k) clearance for Seiler Precision Microscopes. As of , FDA records show no recalls naming K101141.

Clearance record

Decision date
Received
(106 days to decision)
Product code
HEX Colposcope (And Colpomicroscope)
Regulation
21 CFR 884.1630
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Seiler Precision Microscopes 3433 Tree Ct. Industrial Blvd., St. Louis MO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HEX

Trailing 12 months

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

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