Home / 510(k) Clearances / K842766

510(k) K842766

CRYSTAL MEDICAL MILK COLLECTION KIT by Crystal Medical Products, Inc. — Product Code HGX

K842766 is an FDA 510(k) premarket notification submitted by Crystal Medical Products, Inc. for the device "CRYSTAL MEDICAL MILK COLLECTION KIT". The FDA issued a decision of Substantially Equivalent on September 25, 1984. The device falls under product code HGX (Pump, Breast, Powered), a Class II device regulated under 21 CFR 884.5160. Crystal Medical Products, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 1984
Date Received
July 16, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Breast, Powered
Device Class
Class II
Regulation Number
884.5160
Review Panel
OB
Submission Type

Other clearances by Crystal Medical Products, Inc.

  • K861513 — LA DIFFUSION TECHNIQUE, KTY CM-10 BREAST PUMP (August 8, 1986)
  • K853107 — AXICARE CM-14 AUTOMATIC BREAST PUMP (November 19, 1985)
  • K850753 — NATURAL MOTHER BREAST PUMP (June 7, 1985)
  • K850242 — CRYSTAL MANUAL BREAST PUMP (February 25, 1985)

Other clearances for product code HGX

  • K254203 — Wearable Breast Pump (Model S36) (September 17, 2026)
  • K261622 — Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF5 (September 3, 2026)
  • K262774 — Wearable breast pump (Model: XN/MD-2249BS, ZFHF) (September 1, 2026)
  • K260643 — Cimilre Dual Max (August 21, 2026)
  • K261298 — Wearable Electric Breast Pump (YM-8837, YM-8838, YM-8856(H03), YM-8809(S42)) (August 20, 2026)
  • K260259 — DiscreetDuo™ Flow Wearable Breast Pump (Model S3) (July 24, 2026)
  • K261199 — Wearable Breast Pump (Model S32A) (July 13, 2026)
  • K250070 — Electric breast pump (MY-375,MY-376,MY-378,MY-379,MY-380,V3) (June 26, 2026)
  • K261025 — Wearable breast pump (QY-101, QY-102, QY-108) (June 25, 2026)
  • K254254 — Momcozy Wearable Breast Pump (BP311, BP311-A, BP311-B, BP311-C, BP311-D) (June 18, 2026)

FDA data resources