Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ADEL MEDICAL BIRTHING BED, #LD-500

K-Number: K810886 · 1981-04-23

Decision Date1981-04-23
Product CodeHDD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ADEL MEDICAL BIRTHING BED, #LD-500 is the device name listed in this FDA 510(k) record. The listed applicant is Adel Medical , Ltd.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810886. The device is classified under product code HDD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADEL MEDICAL BIRTHING BED, #LD-500?

ADEL MEDICAL BIRTHING BED, #LD-500 is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Adel Medical , Ltd.. The 510(k) number is K810886.

When did ADEL MEDICAL BIRTHING BED, #LD-500 receive FDA 510(k) clearance?

ADEL MEDICAL BIRTHING BED, #LD-500 received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810886.

Who is the listed applicant for ADEL MEDICAL BIRTHING BED, #LD-500?

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 MEDICAL BIRTHING BED, #LD-500?

The FDA product code for ADEL MEDICAL BIRTHING BED, #LD-500 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.

View all 8 devices →

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.

↑