SPECIMEN SET— 510(k) K802340

Substantially Equivalent

American Pharmaseal Div. Ahsc

FDA 510(k) clearance K802340 for SPECIMEN SET, Substantially Equivalent on 1980-10-10. Applicant: American Pharmaseal Div. Ahsc. Device class: 1.

Clearance details

Applicant: American Pharmaseal Div. Ahsc
Product code: Code FMH
Device class: Class 1
Regulation: 21 CFR 864.3250
Advisory panel: Pathology
Date received: 1980-09-26
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FMH

K900983 — TRI-TECH URINE SPECIMEN KIT1990-09-17
K823763 — VARIOUS-SPECIMEN COLLECTORS1983-01-19
K820180 — CALCULI FILTER CUP1982-02-05
K812933 — LANCER SPECIMEN CONTAINER1981-11-06
K802002 — URINE SPECIMEN CONTAINER #'S 1013-10161980-09-09

More clearances from American Pharmaseal Div. Ahsc

K874022 — PHARMASEAL WOUND IRRIGATION DEVICE1987-12-30
K874045 — PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWER1987-12-03
K874517 — PHARMASEAL RUBBER URETHRAL CATHETER1987-12-03
K873359 — AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE1987-11-06
K872228 — PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM1987-09-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.