DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX
K-Number: K092827 · 2010-01-08
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Device Summary
Frequently Asked Questions
What is the DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX?
DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX is a medical device that received FDA 510(k) clearance on 2010-01-08. The listed applicant is Dimeda Instrumente GmbH. The 510(k) number is K092827.
When did DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX receive FDA 510(k) clearance?
DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX received FDA 510(k) clearance on 2010-01-08, under 510(k) number K092827.
Who is the listed applicant for DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX?
The FDA 510(k) record lists Dimeda Instrumente GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX?
The FDA product code for DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX is HDA.
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.
Related Devices (Code: HDA)
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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