K870877 is the FDA 510(k) clearance record for BIO-VENT REUTER BOBBIN TUBE, a class II device, cleared for Richards Medical Co., Inc. on 1987-03-26 under FDA product code ETD (Tube, Tympanostomy). FDA records list 71 510(k) clearances for Richards Medical Co., Inc., from 1983-09-29 to 1990-06-25 . As of 2026-09-10 , FDA records show no recalls naming K870877.
Clearance record Decision date 1987-03-26 Received 1987-03-03 (23 days to decision) Product code ETD Tube, TympanostomyRegulation 21 CFR 874.3880 Device class Class II Review panel Ear, Nose, Throat Applicant Richards Medical Co., Inc. 1450 Brooks Rd., Memphis TN Third party review No
Clearances, product code ETD Trailing 12 months 1 clearance under product code ETD in the twelve months to October 2026, April 2026 the highest month at 1. Show the numbers FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
Product code ETD
Z-0970-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 4,080 units (1510 US, 2570 OUS) Z-0969-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 2,440 units (1940 US, 500 OUS) Z-0968-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 310 units (160 US, 150 OUS) Z-0967-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 5,120 units (2190 US, 2930 OUS) Z-0966-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 6,280 units (2500 US, 3780 OUS) Z-0965-2025 Class II Lack of 510(k) clearance. Adept Medical Ltd / initiated 2024-11-24 / 2,610 units (240 US, 2370 OUS)
MDM coverage of this record lists here, newest first.
About this record Sourced from the FDA 510(k) premarket notification database, ingested from openFDA. MDM adds the decision time in days, the product code cross-link, recalls sharing that product code, and MDM coverage of the record.
Predicate devices are not listed. The openFDA 510(k) endpoint does not publish predicate references, so MDM does not assert them. Where a 510(k) summary exists, the FDA PDF is linked above and names the predicate itself.
Data as of 2026-09-28 , the FDA export date for this dataset. Page last changed 2026-09-05 . View this record on fda.gov ↗ (opens on fda.gov)
