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)

TALLEY MICRO SYSTEM/TALLEY RIPPLEBED

K-Number: K914775 · 1992-04-10

Decision Date1992-04-10
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TALLEY MICRO SYSTEM/TALLEY RIPPLEBED is the device name listed in this FDA 510(k) record. The listed applicant is Talley Group, Ltd.. It received FDA 510(k) clearance on 1992-04-10 under 510(k) number K914775. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALLEY MICRO SYSTEM/TALLEY RIPPLEBED?

TALLEY MICRO SYSTEM/TALLEY RIPPLEBED is a medical device that received FDA 510(k) clearance on 1992-04-10. The listed applicant is Talley Group, Ltd.. The 510(k) number is K914775.

When did TALLEY MICRO SYSTEM/TALLEY RIPPLEBED receive FDA 510(k) clearance?

TALLEY MICRO SYSTEM/TALLEY RIPPLEBED received FDA 510(k) clearance on 1992-04-10, under 510(k) number K914775.

Who is the listed applicant for TALLEY MICRO SYSTEM/TALLEY RIPPLEBED?

The FDA 510(k) record lists Talley Group, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TALLEY MICRO SYSTEM/TALLEY RIPPLEBED?

The FDA product code for TALLEY MICRO SYSTEM/TALLEY RIPPLEBED is FNM.

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 Talley Group, 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: FNM)

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.

↑