PRESPO 7, SELF-SUFFICIENT DRIP DEVICE
K-Number: K933848 · 1995-03-03
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Device Summary
Frequently Asked Questions
What is the PRESPO 7, SELF-SUFFICIENT DRIP DEVICE?
PRESPO 7, SELF-SUFFICIENT DRIP DEVICE is a medical device that received FDA 510(k) clearance on 1995-03-03. The listed applicant is Bonding Corp.. The 510(k) number is K933848.
When did PRESPO 7, SELF-SUFFICIENT DRIP DEVICE receive FDA 510(k) clearance?
PRESPO 7, SELF-SUFFICIENT DRIP DEVICE received FDA 510(k) clearance on 1995-03-03, under 510(k) number K933848.
Who is the listed applicant for PRESPO 7, SELF-SUFFICIENT DRIP DEVICE?
The FDA 510(k) record lists Bonding Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRESPO 7, SELF-SUFFICIENT DRIP DEVICE?
The FDA product code for PRESPO 7, SELF-SUFFICIENT DRIP DEVICE is FPA.
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.
Related Devices (Code: FPA)
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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