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FDA 510(k)

INMAN MEDICAL PACKING STRIP

K-Number: K921291 · 1993-01-21

Decision Date1993-01-21
Product CodeFER
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INMAN MEDICAL PACKING STRIP is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1993-01-21 under 510(k) number K921291. The device is classified under product code FER. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INMAN MEDICAL PACKING STRIP?

INMAN MEDICAL PACKING STRIP is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Inman Medical Corp.. The 510(k) number is K921291.

When did INMAN MEDICAL PACKING STRIP receive FDA 510(k) clearance?

INMAN MEDICAL PACKING STRIP received FDA 510(k) clearance on 1993-01-21, under 510(k) number K921291.

Who is the listed applicant for INMAN MEDICAL PACKING STRIP?

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

What is the FDA product code for INMAN MEDICAL PACKING STRIP?

The FDA product code for INMAN MEDICAL PACKING STRIP is FER.

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 Inman 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.

View all 14 devices →

Related Devices (Code: FER)

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.

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