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FDA 510(k)

COAST MEDICAL, INC. RECTAL PROBE

K-Number: K930930 · 1994-02-25

Decision Date1994-02-25
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COAST MEDICAL, INC. RECTAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Coast Medical Corp.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K930930. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAST MEDICAL, INC. RECTAL PROBE?

COAST MEDICAL, INC. RECTAL PROBE is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Coast Medical Corp.. The 510(k) number is K930930.

When did COAST MEDICAL, INC. RECTAL PROBE receive FDA 510(k) clearance?

COAST MEDICAL, INC. RECTAL PROBE received FDA 510(k) clearance on 1994-02-25, under 510(k) number K930930.

Who is the listed applicant for COAST MEDICAL, INC. RECTAL PROBE?

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

What is the FDA product code for COAST MEDICAL, INC. RECTAL PROBE?

The FDA product code for COAST MEDICAL, INC. RECTAL PROBE is FLL.

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 Coast Medical Corp. 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: FLL)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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