CRYSTAL MANUAL BREAST PUMP
K-Number: K850242 · 1985-02-25
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Device Summary
Frequently Asked Questions
What is the CRYSTAL MANUAL BREAST PUMP?
CRYSTAL MANUAL BREAST PUMP is a medical device that received FDA 510(k) clearance on 1985-02-25. The listed applicant is Crystal Medical Products, Inc.. The 510(k) number is K850242.
When did CRYSTAL MANUAL BREAST PUMP receive FDA 510(k) clearance?
CRYSTAL MANUAL BREAST PUMP received FDA 510(k) clearance on 1985-02-25, under 510(k) number K850242.
Who is the listed applicant for CRYSTAL MANUAL BREAST PUMP?
The FDA 510(k) record lists Crystal Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CRYSTAL MANUAL BREAST PUMP?
The FDA product code for CRYSTAL MANUAL BREAST PUMP is HGY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Crystal Medical Products, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HGY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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