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)

CPR C-SECTION DELIVERY PACK

K-Number: K960243 · 1996-05-23

Decision Date1996-05-23
Product CodeMLS
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CPR C-SECTION DELIVERY PACK is the device name listed in this FDA 510(k) record. The listed applicant is Custom Pack Reliability. It received FDA 510(k) clearance on 1996-05-23 under 510(k) number K960243. The device is classified under product code MLS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR C-SECTION DELIVERY PACK?

CPR C-SECTION DELIVERY PACK is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Custom Pack Reliability. The 510(k) number is K960243.

When did CPR C-SECTION DELIVERY PACK receive FDA 510(k) clearance?

CPR C-SECTION DELIVERY PACK received FDA 510(k) clearance on 1996-05-23, under 510(k) number K960243.

Who is the listed applicant for CPR C-SECTION DELIVERY PACK?

The FDA 510(k) record lists Custom Pack Reliability as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPR C-SECTION DELIVERY PACK?

The FDA product code for CPR C-SECTION DELIVERY PACK is MLS.

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 Custom Pack Reliability 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 21 devices →

Related Devices (Code: MLS)

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.

↑