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)

CINCH STRAP WITH BUCKLE

K-Number: K963370 · 1996-11-08

Decision Date1996-11-08
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CINCH STRAP WITH BUCKLE is the device name listed in this FDA 510(k) record. The listed applicant is Morrison Medical Products. It received FDA 510(k) clearance on 1996-11-08 under 510(k) number K963370. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CINCH STRAP WITH BUCKLE?

CINCH STRAP WITH BUCKLE is a medical device that received FDA 510(k) clearance on 1996-11-08. The listed applicant is Morrison Medical Products. The 510(k) number is K963370.

When did CINCH STRAP WITH BUCKLE receive FDA 510(k) clearance?

CINCH STRAP WITH BUCKLE received FDA 510(k) clearance on 1996-11-08, under 510(k) number K963370.

Who is the listed applicant for CINCH STRAP WITH BUCKLE?

The FDA 510(k) record lists Morrison Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CINCH STRAP WITH BUCKLE?

The FDA product code for CINCH STRAP WITH BUCKLE is FMQ.

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 Morrison Medical Products 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: FMQ)

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.

↑