CULTURE COLLEC. TRANS. SYS., DOUBLE DRY
K-Number: K772209 · 1977-12-20
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Device Summary
Frequently Asked Questions
What is the CULTURE COLLEC. TRANS. SYS., DOUBLE DRY?
CULTURE COLLEC. TRANS. SYS., DOUBLE DRY is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K772209.
When did CULTURE COLLEC. TRANS. SYS., DOUBLE DRY receive FDA 510(k) clearance?
CULTURE COLLEC. TRANS. SYS., DOUBLE DRY received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772209.
Who is the listed applicant for CULTURE COLLEC. TRANS. SYS., DOUBLE DRY?
The FDA 510(k) record lists Precision Dynamics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CULTURE COLLEC. TRANS. SYS., DOUBLE DRY?
The FDA product code for CULTURE COLLEC. TRANS. SYS., DOUBLE DRY is JTW.
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 Precision Dynamics 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: JTW)
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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