ADEL MODEL 2100 BIRTHING BED
K-Number: K874610 · 1988-01-21
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Device Summary
Frequently Asked Questions
What is the ADEL MODEL 2100 BIRTHING BED?
ADEL MODEL 2100 BIRTHING BED is a medical device that received FDA 510(k) clearance on 1988-01-21. The listed applicant is Adel Medical , Ltd.. The 510(k) number is K874610.
When did ADEL MODEL 2100 BIRTHING BED receive FDA 510(k) clearance?
ADEL MODEL 2100 BIRTHING BED received FDA 510(k) clearance on 1988-01-21, under 510(k) number K874610.
Who is the listed applicant for ADEL MODEL 2100 BIRTHING BED?
The FDA 510(k) record lists Adel Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADEL MODEL 2100 BIRTHING BED?
The FDA product code for ADEL MODEL 2100 BIRTHING BED is HDD.
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 Adel Medical , Ltd. 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: HDD)
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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